46 results on '"Michael A. Massiah"'
Search Results
2. B-box1 Domain of MID1 Interacts with the Ube2D1 E2 Enzyme Differently Than RING E3 Ligases
- Author
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Anupreet Kaur, Erin M. Gladu, Katharine M. Wright, Jessica A. Webb, and Michael A. Massiah
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Biochemistry - Published
- 2023
3. Molecular dynamics simulation reveals insights into the mechanism of unfolding by the A130T/V mutations within the MID1 zinc-binding Bbox1 domain.
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Yunjie Zhao, Chen Zeng, and Michael A Massiah
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Medicine ,Science - Abstract
The zinc-binding Bbox1 domain in protein MID1, a member of the TRIM family of proteins, facilitates the ubiquitination of the catalytic subunit of protein phosphatase 2A and alpha4, a protein regulator of PP2A. The natural mutation of residue A130 to a valine or threonine disrupts substrate recognition and catalysis. While NMR data revealed the A130T mutant Bbox1 domain failed to coordinate both structurally essential zinc ions and resulted in an unfolded structure, the unfolding mechanism is unknown. Principle component analysis revealed that residue A130 served as a hinge point between the structured β-strand-turn-β-strand (β-turn-β) and the lasso-like loop sub-structures that constitute loop1 of the ββα-RING fold that the Bbox1 domain adopts. Backbone RMSD data indicate significant flexibility and departure from the native structure within the first 5 ns of the molecular dynamics (MD) simulation for the A130V mutant (>6 Å) and after 30 ns for A130T mutant (>6 Å). Overall RMSF values were higher for the mutant structures and showed increased flexibility around residues 125 and 155, regions with zinc-coordinating residues. Simulated pKa values of the sulfhydryl group of C142 located near A130 suggested an increased in value to ~9.0, paralleling the increase in the apparent dielectric constants for the small cavity near residue A130. Protonation of the sulfhydryl group would disrupt zinc-coordination, directly contributing to unfolding of the Bbox1. Together, the increased motion of residues of loop 1, which contains four of the six zinc-binding cysteine residues, and the increased pKa of C142 could destabilize the structure of the zinc-coordinating residues and contribute to the unfolding.
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- 2015
- Full Text
- View/download PDF
4. Anti-Platelet Effect Induced by Iron Oxide Nanoparticles: Correlation with Conformational Change in Fibrinogen
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Brian Schnoor, Regina Komal Kottana, Anne-Laure Papa, Nadine Millot, Michael A. Massiah, Jessica Ann Webb, Lionel Maurizi, Kenise Morris, Laboratoire Interdisciplinaire Carnot de Bourgogne (LICB), and Université de Bourgogne (UB)-Centre National de la Recherche Scientifique (CNRS)
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Conformational change ,Protein Corona ,antiplatelet effect ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Polyvinyl alcohol ,Ferric Compounds ,Biomaterials ,chemistry.chemical_compound ,Humans ,General Materials Science ,Platelet ,Platelet activation ,[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics ,Magnetite Nanoparticles ,ComputingMilieux_MISCELLANEOUS ,superparamagnetic iron oxide nanoparticles ,Fibrinogen ,General Chemistry ,021001 nanoscience & nanotechnology ,Blood proteins ,0104 chemical sciences ,chemistry ,Hemostasis ,Polyvinyl Alcohol ,platelets ,Biophysics ,nanoparticle-protein interactions ,Magnetic Iron Oxide Nanoparticles ,0210 nano-technology ,Iron oxide nanoparticles ,Biotechnology - Abstract
Iron oxide nanoparticles are developed for various biomedical applications, however, there is limited understanding regarding their effects and toxicity on blood components. The particles traveling in circulation inevitably interact with blood cells and plasma proteins and may interfere with hemostasis. Specifically, this study focuses on the influence of superparamagnetic iron oxide nanoparticles (SPIONs) coated with a biocompatible polymer, polyvinyl alcohol (PVA), on platelet function. Here, engineered SPIONs that are functionalized with various PVA coatings to provide these particles with different surface charges and polymer packing are described. These formulations are assessed for any interference with human platelet functions and coagulation, ex vivo. Positively charged SPIONs induce a significant change in platelet GPIIb-IIIa conformation, indicative of platelet activation at the dose of 500 µg mL-1 . Remarkably, engineered PVA(polyvinyl alcohol)-SPIONs all display a robust dose-dependent anti-platelet effect on platelet aggregation, regardless of the PVA charge and molecular weight. After assessing hypotheses involving SPION-induced steric hindrance in platelet-platelet bridging, as well as protein corona involvement in the antiplatelet effect, the study concludes that the presence of PVA-SPIONs induces fibrinogen conformational change, which correlates with the observed dose-dependent anti-platelet effect.
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- 2020
5. NMR studies of the C-terminus of alpha4 reveal possible mechanism of its interaction with MID1 and protein phosphatase 2A.
- Author
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Haijuan Du and Michael A Massiah
- Subjects
Medicine ,Science - Abstract
Alpha4 is a regulatory subunit of the protein phosphatase family of enzymes and plays an essential role in regulating the catalytic subunit of PP2A (PP2Ac) within the rapamycin-sensitive signaling pathway. Alpha4 also interacts with MID1, a microtubule-associated ubiquitin E3 ligase that appears to regulate the function of PP2A. The C-terminal region of alpha4 plays a key role in the binding interaction of PP2Ac and MID1. Here we report on the solution structure of a 45-amino acid region derived from the C-terminus of alpha4 (alpha45) that binds tightly to MID1. In aqueous solution, alpha45 has properties of an intrinsically unstructured peptide although chemical shift index and dihedral angle estimation based on chemical shifts of backbone atoms indicate the presence of a transient α-helix. Alpha45 adopts a helix-turn-helix HEAT-like structure in 1% SDS micelles, which may mimic a negatively charged surface for which alpha45 could bind. Alpha45 binds tightly to the Bbox1 domain of MID1 in aqueous solution and adopts a structure consistent with the helix-turn-helix structure observed in 1% SDS. The structure of alpha45 reveals two distinct surfaces, one that can interact with a negatively charged surface, which is present on PP2A, and one that interacts with the Bbox1 domain of MID1.
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- 2011
- Full Text
- View/download PDF
6. Structural and functional observations of the P151L MID1 mutation reveal alpha4 plays a significant role in X-linked Opitz Syndrome
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Katharine M. Wright, Michael A. Massiah, and Haijuan Du
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Models, Molecular ,0301 basic medicine ,Ubiquitin-Protein Ligases ,Protein subunit ,Regulator ,medicine.disease_cause ,Biochemistry ,Substrate Specificity ,03 medical and health sciences ,Esophagus ,Protein Domains ,Ubiquitin ,medicine ,Humans ,Amino Acid Sequence ,Protein Phosphatase 2 ,Molecular Biology ,Zinc finger ,Genetics ,Hypospadias ,Mutation ,Hypertelorism ,Sequence Homology, Amino Acid ,biology ,Ubiquitination ,Nuclear Proteins ,Genetic Diseases, X-Linked ,Cell Biology ,Protein phosphatase 2 ,Protein tertiary structure ,Protein Structure, Tertiary ,Ubiquitin ligase ,Cleft Palate ,030104 developmental biology ,embryonic structures ,Microtubule Proteins ,biology.protein ,Protein Processing, Post-Translational ,Transcription Factors - Abstract
Mutations of human MID1 are associated with X-linked Opitz G Syndrome (XLOS), which is characterized by midline birth defects. XLOS-observed mutations within the MID1 B-box1 domain are associated with cleft lip/palate, wide-spaced eyes and hyperspadias. Three of the four XLOS-observed mutations in the B-box1 domain results in unfolding but the structural and functional effects of the P151L mutation is not characterized. Here, we demonstrate that the P151L mutation does not disrupt the overall tertiary structure of the B-box1 domain and the adjacent domains. In fact, MID1 E3 ligase activity is slightly enhanced. However, the P151L mutation disrupted the ability of MID1 to catalyze the poly-ubiquitination of alpha4, a novel regulator of PP2A. This observation is consistent with results observed with the other three structure-destabilizing B-box1 mutations in targeting alpha4 but not PP2A. Alpha4 is shown to bind and sequester the catalytic subunit of PP2A and protect it from MID1-mediated ubiquitination and as a result, an increase in alpha4 can contribute to an increase in PP2A, playing a greater role in midline development during embryogenesis.
- Published
- 2017
7. Zinc-Binding B-Box Domains with RING Folds Serve Critical Roles in the Protein Ubiquitination Pathways in Plants and Animals
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Michael A. Massiah
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Zinc binding ,Chemistry ,Ring (chemistry) ,Protein ubiquitination ,Cell biology - Published
- 2019
8. Anti‐Platelet Effect: Anti‐Platelet Effect Induced by Iron Oxide Nanoparticles: Correlation with Conformational Change in Fibrinogen (Small 1/2021)
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Brian Schnoor, Lionel Maurizi, Michael A. Massiah, Kenise Morris, Nadine Millot, Anne-Laure Papa, Regina Komal Kottana, and Jessica Ann Webb
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Conformational change ,Superparamagnetic iron oxide nanoparticles ,General Chemistry ,Fibrinogen ,Anti platelet ,Polyvinyl alcohol ,Biomaterials ,chemistry.chemical_compound ,chemistry ,medicine ,Biophysics ,General Materials Science ,Platelet ,Iron oxide nanoparticles ,Biotechnology ,medicine.drug - Published
- 2021
9. Solution structure of the microtubule‐targeting COS domain of MID1
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Mesgana Dagnachew, Michael A. Massiah, Katharine M. Wright, and Haijuan Du
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Models, Molecular ,Protein Conformation, alpha-Helical ,0301 basic medicine ,EGF-like domain ,Ubiquitin-Protein Ligases ,Protein domain ,Protein Data Bank (RCSB PDB) ,Biology ,Microtubules ,Biochemistry ,03 medical and health sciences ,0302 clinical medicine ,Protein Domains ,Microtubule ,Humans ,Nuclear Magnetic Resonance, Biomolecular ,Molecular Biology ,chemistry.chemical_classification ,DNA ligase ,Nuclear Proteins ,Cell Biology ,Protein phosphatase 2 ,Ubiquitin ligase ,030104 developmental biology ,chemistry ,Cyclic nucleotide-binding domain ,Microtubule Proteins ,biology.protein ,Biophysics ,030217 neurology & neurosurgery ,Transcription Factors - Abstract
UNLABELLED The human MID1 protein is required for the proper development during embryogenesis. Mutations of MID1 are associated with X-linked Opitz G syndrome, characterized by midline anomalies. MID1 associates with the microtubules and functions as an ubiquitin E3 ligase, targeting protein phosphatase 2A for ubiquitin-mediated regulation. The mechanism of microtubule association is not known. Recently, a 60-amino acid region termed the C-terminal subgroup One Signature (COS) box/domain was identified at the C-terminal end of the coiled-coil (CC) domain that facilitates microtubule localization. Insertion of the MID1 COS domain at the C-terminal end of the CC domain of a nonmicrotubule-associated TRIM protein confers microtubule localization. Here, we report the solution structure of the COS domain of MID1. The domain adopts a helix-loop-helix structure in which the N- and C-terminal ends are in close proximity. Hydrophobic residues stabilizing the interaction of the two α-helices form a central hydrophobic core. The loop separating the α-helices is structured, with two of its hydrophobic residues making contact with the central core. On the outer surface, positively charged residues form a distinct basic patch near the termini that we postulate is important for microtubule binding. A model of the structure of the preceding coiled-coil and COS domains (CC-COS) show that the COS domain forms a helical bundle at the C-terminal end of the CC domain similar to the spectrin-like fold observed with some known microtubule-binding proteins. Interestingly, the CC-COS domains bind to microtubules, demonstrating for the first time that MID1 can directly associate with the microtubules. DATABASE Structural data are available in PDB database under the accession number 5IM8.
- Published
- 2016
10. The Diversity of Chemoprotective Glucosinolates in Moringaceae (Moringa spp.)
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Walter C. Hubbard, Mark E. Olson, Gwen M. Chodur, Kristina L. Wade, Katherine K. Stephenson, Jed W. Fahey, David W. Odee, Wasif Nouman, Patricia A. Egner, Michael A. Massiah, and Jesse Alt
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0301 basic medicine ,Exudate ,Magnetic Resonance Spectroscopy ,Glucosinolates ,lcsh:Medicine ,Biology ,Chemoprevention ,Mass Spectrometry ,Article ,Moringa ,03 medical and health sciences ,Botany ,medicine ,Humans ,lcsh:Science ,Cells, Cultured ,Phylogeny ,Moringa oleifera ,Multidisciplinary ,Plant Extracts ,lcsh:R ,Interspecific competition ,Plant Leaves ,030104 developmental biology ,Cytoprotection ,Chronic Disease ,Seeds ,Chemoprotective ,lcsh:Q ,medicine.symptom ,Phytotherapy - Abstract
Glucosinolates (GS) are metabolized to isothiocyanates that may enhance human healthspan by protecting against a variety of chronic diseases. Moringa oleifera, the drumstick tree, produces unique GS but little is known about GS variation within M. oleifera, and even less in the 12 other Moringa species, some of which are very rare. We assess leaf, seed, stem, and leaf gland exudate GS content of 12 of the 13 known Moringa species. We describe 2 previously unidentified GS as major components of 6 species, reporting on the presence of simple alkyl GS in 4 species, which are dominant in M. longituba. We document potent chemoprotective potential in 11 of 12 species, and measure the cytoprotective activity of 6 purified GS in several cell lines. Some of the unique GS rank with the most powerful known inducers of the phase 2 cytoprotective response. Although extracts of most species induced a robust phase 2 cytoprotective response in cultured cells, one was very low (M. longituba), and by far the highest was M. arborea, a very rare and poorly known species. Our results underscore the importance of Moringa as a chemoprotective resource and the need to survey and conserve its interspecific diversity.
- Published
- 2018
11. The MID1 E3 Ligase Catalyzes the Polyubiquitination of Alpha4 (α4), a Regulatory Subunit of Protein Phosphatase 2A (PP2A)
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Haijuan Du, Erica Walters, Timothy C. Cox, Michael A. Massiah, Yongzhao Huang, and Manar Zaghlula
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biology ,Protein subunit ,Lactacystin ,Cell Biology ,Protein phosphatase 2 ,Protein degradation ,Biochemistry ,Ubiquitin ligase ,chemistry.chemical_compound ,chemistry ,Ubiquitin ,Proteasome inhibitor ,medicine ,biology.protein ,Monoubiquitination ,Molecular Biology ,medicine.drug - Abstract
Alpha4 (α4) is a key regulator of protein phosphatase 2A (PP2A) and mTOR in steps essential for cell-cycle progression. α4 forms a complex with PP2A and MID1, a microtubule-associated ubiquitin E3 ligase that facilitates MID1-dependent regulation of PP2A and the dephosphorylation of MID1 by PP2A. Ectopic overexpression of α4 is associated with hepatocellular carcinomas, breast cancer, and invasive adenocarcinomas. Here, we provide data suggesting that α4 is regulated by ubiquitin-dependent degradation mediated by MID1. In cells stably expressing a dominant-negative form of MID1, significantly elevated levels of α4 were observed. Treatment of cells with the specific proteasome inhibitor, lactacystin, resulted in a 3-fold increase in α4 in control cells and a similar level in mutant cells. Using in vitro assays, individual MID1 E3 domains facilitated monoubiquitination of α4, whereas full-length MID1 as well as RING-Bbox1 and RING-Bbox1-Bbox2 constructs catalyzed its polyubiquitination. In a novel non-biased functional screen, we identified a leucine to glutamine substitution at position 146 within Bbox1 that abolished MID1-α4 interaction and the subsequent polyubiquitination of α4, indicating that direct binding to Bbox1 was necessary for the polyubiquitination of α4. The mutant had little impact on the RING E3 ligase functionality of MID1. Mass spectrometry data confirmed Western blot analysis that ubiquitination of α4 occurs only within the last 105 amino acids. These novel findings identify a new role for MID1 and a mechanism of regulation of α4 that is likely to impact the stability and activity level of PP2Ac.
- Published
- 2013
12. Obtaining Soluble Folded Proteins from Inclusion Bodies Using Sarkosyl, Triton X‐100, and CHAPS: Application to LB and M9 Minimal Media
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Katharine M. Wright, Michael A. Massiah, and Haijuan Du
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0301 basic medicine ,Protein Folding ,Lysis ,Octoxynol ,Recombinant Fusion Proteins ,Protein Engineering ,Biochemistry ,Inclusion bodies ,law.invention ,03 medical and health sciences ,chemistry.chemical_compound ,Affinity chromatography ,Structural Biology ,Chaps ,law ,Escherichia coli ,Sorbitol ,Histidine ,Glutathione Transferase ,Inclusion Bodies ,Chromatography ,030102 biochemistry & molecular biology ,Cholic Acids ,Sarcosine ,Fusion protein ,Recombinant Proteins ,Betaine ,030104 developmental biology ,Solubility ,chemistry ,Solubilization ,Triton X-100 ,Recombinant DNA - Abstract
This unit describes a straightforward and efficient method of using sarkosyl to solubilize and recover difficult recombinant proteins, such as GST- and His6 -tagged fusion proteins, that are overexpressed in E. coli. This protocol is especially useful for rescuing recombinant proteins overexpressed in M9 minimal medium. Sarkosyl added to lysis buffers helps with both protein solubility and cell lysis. Higher percentage sarkosyl (up to 10%) can extract >95% of soluble protein from inclusion bodies. In the case of sarkosyl-solubilized GST-fusion proteins, batch-mode affinity purification requires addition of a specific ratio of Triton X-100 and CHAPS, while sarkosyl-solubilized His6 -tagged fusion proteins can be directly purified on Ni(2+) resin columns. Proteins purified by this method could be widely used in biological assays, structure analysis and mass spectrum assay.
- Published
- 2016
13. Purifying natively folded proteins from inclusion bodies using sarkosyl, Triton X-100, and CHAPS
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Wenjun Liu, Timothy C. Cox, Helen K Harris, Hu Tao, Michael A. Massiah, and Brandi Simmons
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Protein Folding ,Octoxynol ,Recombinant Fusion Proteins ,Maltose-Binding Proteins ,General Biochemistry, Genetics and Molecular Biology ,Inclusion bodies ,Sepharose ,chemistry.chemical_compound ,Maltose-binding protein ,Chaps ,Escherichia coli ,Glutathione Transferase ,Inclusion Bodies ,biology ,Cholic Acids ,Sarcosine ,Glutathione ,Fusion protein ,Solubility ,chemistry ,Biochemistry ,Solubilization ,Periplasmic Binding Proteins ,Triton X-100 ,biology.protein ,Biotechnology - Abstract
We describe a rapid, simple, and efficient method for recovering glutathione S-transferase (GST)- and His6-tagged maltose binding protein (MBP) fusion proteins from inclusion bodies. Incubation of inclusion bodies with 10% sarkosyl effectively solubilized >95% of proteins, while high-yield recovery of sarkosyl-solubilized fusion proteins was obtained with a specific ratio of Triton X-100 and CHAPS. We demonstrate for the first time that this combination of three detergents significantly improves binding efficiency of GST and GST fusion proteins to gluthathione (GSH) Sepharose.
- Published
- 2010
14. Structure of the MID1 Tandem B-Boxes Reveals an Interaction Reminiscent of Intermolecular Ring Heterodimers
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Suryaparkash Singireddy, Madhu Jakkidi, Timothy C. Cox, Michael A. Massiah, Hu Tao, Brandi Simmons, and Kieran M. Short
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Models, Molecular ,Repetitive Sequences, Amino Acid ,Protein Folding ,Protein family ,Ubiquitin-Protein Ligases ,Protein subunit ,Plasma protein binding ,Biochemistry ,Protein Structure, Secondary ,Protein structure ,Humans ,Protein Structure, Quaternary ,chemistry.chemical_classification ,DNA ligase ,Tandem ,biology ,Nuclear Proteins ,Protein Structure, Tertiary ,Ubiquitin ligase ,Crystallography ,chemistry ,Microtubule Proteins ,Mutagenesis, Site-Directed ,biology.protein ,Protein folding ,Dimerization ,Protein Binding ,Transcription Factors - Abstract
The tripartite motif (TRIM) protein family, defined by N-terminal RING, B-box, and coiled-coil (RBCC) domains, consists of either a single type 2 B-box domain or tandem B-box domains of type 1 and type 2 (B1B2). Here, we report the first structure of the B-box domains in their native tandem orientation. The B-boxes are from Midline-1, a putative ubiquitin E3 ligase that is required for the proteosomal degradation of the catalytic subunit of protein phosphatase 2A (PP2Ac). This function of MID1 is facilitated by the direct binding of Alpha4, a regulatory subunit of PP2Ac, to B-box1, while B-box2 appears to influence this interaction. Both B-box1 and B-box2 bind two zinc atoms in a cross-brace motif and adopt a similar betabetaalpha structure reminiscent of the RING, PHD, ZZ, and U-box domains, although they differ from each other and with RING domains in the spacing of their zinc-binding residues. The two B-box domains pack against each other with the interface formed by residues located on the structured loop consisting of the two antiparallel beta-strands. The surface area of the interface is 188 A2 (17% of the total surface). Consistent with the globular structure, the Tm of the tandem B-box domain (59 degrees C) is higher than the individual domains, supporting a stable interaction between the B-box 1 and 2 domains. Notably, the interaction is reminiscent of the interaction of recently determined RING dimers, suggesting the possibility of an evolutionarily conserved role for B-box2 domains in regulating functional RING-type folds.
- Published
- 2008
15. The structure and behavior of the NA-CATH antimicrobial peptide with liposomes
- Author
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Susan D. Gillmor, Haijuan Du, Robin Samuel, and Michael A. Massiah
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Models, Molecular ,Protein–liposome interaction ,Fluorophore ,Arginine ,Protein Conformation ,Lysine ,Amphipathic helix ,Molecular Sequence Data ,Biophysics ,Peptide ,Biochemistry ,03 medical and health sciences ,chemistry.chemical_compound ,Structure-Activity Relationship ,Cathelicidins ,Computer Simulation ,Amino Acid Sequence ,030304 developmental biology ,AMP ,chemistry.chemical_classification ,0303 health sciences ,Liposome ,Binding Sites ,030306 microbiology ,Bilayer ,Cell Biology ,Peptide structure ,Amino acid ,Antibacterial ,Membrane ,chemistry ,Models, Chemical ,Liposomes ,NMR structure ,Antimicrobial ,Fluorescence requenching ,NA-CATH ,Protein Binding - Abstract
Naja atra cathelicidin (NA-CATH) is a 34-amino acid highly cationic peptide identified in Chinese cobras to possess potent toxicity against gram-negative and gram-positive bacteria and low toxicity against host cells. Here, we report the NMR solution structure of the full-length NA-CATH peptide and its interaction with liposomes. The structure shows a well-defined α-helix between residues Phe3 to Lys23, on which one surface is lined by the side-chains of one arginine and 11 lysine residues, while the other side is populated by hydrophobic residues. The last eleven amino acids, which are predominately aromatic and hydrophobic in nature, have no defined structure. NMR data reveal that these residues do not interact with the hydrophobic residues of the helix, indicating that the C-terminal residues have random conformations. Fluorescence requenching experiments, in which liposomes serve as a mimic of the bacterial membranes, result in fluorophore leakage that is consistent with a membrane thinning or transient pore formation mechanism. NMR titration studies of the peptide–liposome interaction reveal that the peptide is in fast exchange with the liposome, consistent with the fluorescent studies. These data indicate that full length NA-CATH possesses a helical segment and unstructured C-terminal tail that disrupts the bilayer to induce leakage and lysing.
- Published
- 2015
16. Molecular Dynamics Simulation Reveals Insights into the Mechanism of Unfolding by the A130T/V Mutations within the MID1 Zinc-Binding Bbox1 Domain
- Author
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Michael A. Massiah, Yunjie Zhao, and Chen Zeng
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Models, Molecular ,Protein Folding ,Stereochemistry ,Protein subunit ,Science ,Ubiquitin-Protein Ligases ,Mutant ,Plasma protein binding ,Molecular Dynamics Simulation ,Protein structure ,Humans ,Protein Phosphatase 2 ,Threonine ,Multidisciplinary ,Chemistry ,Ubiquitination ,Nuclear Proteins ,Protein phosphatase 2 ,Protein Structure, Tertiary ,Zinc ,Biochemistry ,Mutation ,Microtubule Proteins ,Medicine ,Protein folding ,Cysteine ,Research Article ,Protein Binding ,Transcription Factors - Abstract
The zinc-binding Bbox1 domain in protein MID1, a member of the TRIM family of proteins, facilitates the ubiquitination of the catalytic subunit of protein phosphatase 2A and alpha4, a protein regulator of PP2A. The natural mutation of residue A130 to a valine or threonine disrupts substrate recognition and catalysis. While NMR data revealed the A130T mutant Bbox1 domain failed to coordinate both structurally essential zinc ions and resulted in an unfolded structure, the unfolding mechanism is unknown. Principle component analysis revealed that residue A130 served as a hinge point between the structured β-strand-turn-β-strand (β-turn-β) and the lasso-like loop sub-structures that constitute loop1 of the ββα-RING fold that the Bbox1 domain adopts. Backbone RMSD data indicate significant flexibility and departure from the native structure within the first 5 ns of the molecular dynamics (MD) simulation for the A130V mutant (>6 A) and after 30 ns for A130T mutant (>6 A). Overall RMSF values were higher for the mutant structures and showed increased flexibility around residues 125 and 155, regions with zinc-coordinating residues. Simulated pKa values of the sulfhydryl group of C142 located near A130 suggested an increased in value to ~9.0, paralleling the increase in the apparent dielectric constants for the small cavity near residue A130. Protonation of the sulfhydryl group would disrupt zinc-coordination, directly contributing to unfolding of the Bbox1. Together, the increased motion of residues of loop 1, which contains four of the six zinc-binding cysteine residues, and the increased pKa of C142 could destabilize the structure of the zinc-coordinating residues and contribute to the unfolding.
- Published
- 2015
17. Solution Structure of the RBCC/TRIM B-box1 Domain of Human MID1: B-box with a RING
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Kieran M. Short, Timothy C. Cox, Michael A. Massiah, and Brandi Simmons
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Sequence Homology, Amino Acid ,Chemistry ,Ubiquitin-Protein Ligases ,Protein subunit ,Molecular Sequence Data ,Nuclear Proteins ,Zinc Fingers ,Nuclear Overhauser effect ,Ring (chemistry) ,Protein Structure, Tertiary ,Solutions ,Zinc ,Crystallography ,Structural Biology ,Domain (ring theory) ,Microtubule Proteins ,Humans ,Amino Acid Sequence ,Molecular Biology ,Two-dimensional nuclear magnetic resonance spectroscopy ,Heteronuclear single quantum coherence spectroscopy ,Histidine ,Transcription Factors ,Cysteine - Abstract
B-box domains are a defining feature of the tripartite RBCC (RING, B-box, coiled-coil) or TRIM proteins, many of which are E3 ubiquitin ligases. However, little is known about the biological function of B-boxes. In some RBCC/TRIM proteins there is only a single B-box (type 2) domain, while others have both type 1 and type 2 B-box domains in tandem adjacent to their RING domain. These two types of B-boxes share little sequence similarity, except the presence of cysteine and histidine residues: eight in most B-box1 domains and seven in B-box2 domains. We report here the high-resolution solution structure of the first B-box1 domain (from the human RBCC protein, MID1) based on 670 nuclear Overhauser effect (NOE)-derived distance restraints, 12 hydrogen bonds, and 44 dihedral angles. The domain consists of a three-turn alpha-helix, two short beta-strands, and three beta-turns, encompassing Val117 to Pro164, which binds two zinc atoms. One zinc atom is coordinated by cysteine residues 119, 122, 142, 145, while cysteine 134, 137 and histidine 150, 159 coordinate the other. This topology is markedly different from the only other B-box structure reported; that of a type 2 B-box from Xenopus XNF7, which binds a single zinc atom. Of note, the B-box1 structure closely resembles the folds of the RING, ZZ and U-box domains of E3 and E4 ubiquitin enzymes, raising the possibility that the B-box1 domain either has E3 activity itself or enhances the activity of RING type E3 ligases (i.e. confers E4 enzyme activity). The structure of the MID1 B-box1 also reveals two potential protein interaction surfaces. One of these is likely to provide the binding interface for Alpha 4 that is required for the localized turnover of the catalytic subunit of PP2A, the major Ser/Thr phosphatase.
- Published
- 2006
18. Solution structure, mutagenesis, and NH exchange studies of the MutT enzyme–Mg2+-8-oxo-dGMP complex
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Albert S. Mildvan, Michael A. Massiah, Hugo F. Azurmendi, and V. Saraswat
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chemistry.chemical_classification ,biology ,Hydrogen bond ,Chemistry ,Stereochemistry ,Organic Chemistry ,Mutant ,Wild type ,Active site ,Pyrophosphate ,Analytical Chemistry ,Inorganic Chemistry ,chemistry.chemical_compound ,Nucleoside triphosphate ,biology.protein ,Nucleotide ,Spectroscopy ,Heteronuclear single quantum coherence spectroscopy - Abstract
The MutT pyrophosphohydrolase from E. coli (129 residues) catalyzes the hydrolysis of nucleoside triphosphates (NTP), including 8-oxo-dGTP, by substitution at Pβ, to yield NMP and pyrophosphate. The product, 8-oxo-dGMP is an unusually tight binding, slowly exchanging inhibitor with a KD=52 nM, (ΔG°=−9.8 kcal/mol) which is 6.1 kcal/mol tighter than the binding of dGMP (ΔG°=−3.7 kcal/mol). The higher affinity for 8-oxo-dGMP results from a more favorable ΔHbinding (−32 kcal/mol) despite an unfavorable −TΔS°binding (+22 kcal/mol). The solution structure of the MutT–Mg2+-8-oxo-dGMP complex shows a narrowed, hydrophobic nucleotide-binding cleft with Asn-119 and Arg-78 among the few polar residues. The N119A, N119D, R78K and R78A single mutations, and the R78K+N119A double mutant all showed largely intact active sites, on the basis of small changes in the kinetic parameters of dGTP hydrolysis and in 1H–15N HSQC spectra. However, the N119A mutation profoundly weakened the active site binding of 8-oxo-dGMP by 4.3 kcal/mol (1650-fold). The N119D mutation also weakened 8-oxo-dGMP binding but only by 2.1 kcal/mol (37-fold), suggesting that Asn-119 functioned both as a hydrogen bond donor to C8O, and a hydrogen bond acceptor from N7H of 8-oxo-dGMP, while aspartate at position −119 functioned as an acceptor of a single hydrogen bond. Much smaller weakening effects (0.3–0.4 kcal/mol) on the binding of dGMP and dAMP were found, indicating specific hydrogen bonding of Asn-119 to 8-oxo-dGMP. While formation of the wild type MutT–Mg2+-8-oxo-dGMP complex slowed the backbone NH exchange rates of 45 residues distributed throughout the protein, the same complex of the N119A mutant slowed the exchange rates of only 11 residues at or near the active site, indicating an increase in conformational flexibility of the N119A mutant. The R78K and R78A mutations weakened the binding of 8-oxo-dGMP by 1.7 and 1.1 kcal/mol, respectively, indicating a lesser role of Arg-78 than of Asn-119 in the selective binding of 8-oxo-dGMP, likely donating a single hydrogen bond to its C6O. The R78K+N119A double mutant weakened the binding of 8-oxo-dGMP (KIslope=3.1 mM) by 6.5±0.2 kcal/mol which overlaps, within error with the sum of the effects of the two single mutants (6.0±0.3 kcal/mol). Such additive effects of the two single mutants in the double mutant are most simply explained by the independent functioning of Asn-119 and Arg-78 in the binding of 8-oxo-dGMP. Independent functioning of these two residues in nucleotide binding is consistent with their locations in the MutT–Mg2+-8-oxo-dGMP complex, on opposite sides of the active site cleft, with a distance of 8.4±0.5 A between their side chain nitrogens.
- Published
- 2004
19. The Roles of Active-Site Residues in the Catalytic Mechanism of trans-3-Chloroacrylic Acid Dehalogenase: A Kinetic, NMR, and Mutational Analysis
- Author
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Michael A. Massiah, Albert S. Mildvan, Susan C. Wang, Hugo F. Azurmendi, Gerrit J. Poelarends, and Christian P. Whitman
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Proline ,Double bond ,Hydrolases ,Stereochemistry ,DNA Mutational Analysis ,Glycine ,Arginine ,Biochemistry ,Catalysis ,chemistry.chemical_compound ,Catalytic Domain ,Pseudomonas ,Binding site ,Nuclear Magnetic Resonance, Biomolecular ,Dehalogenase ,chemistry.chemical_classification ,Binding Sites ,Nitrogen Isotopes ,biology ,Active site ,Hydrogen-Ion Concentration ,Peptide Fragments ,Intramolecular Oxidoreductases ,Kinetics ,Protein Subunits ,Malonate ,Acrylates ,Models, Chemical ,chemistry ,Mutagenesis, Site-Directed ,Solvents ,biology.protein ,Titration ,Protons ,Heteronuclear single quantum coherence spectroscopy - Abstract
trans-3-Chloroacrylic acid dehalogenase (CaaD) converts trans-3-chloroacrylic acid to malonate semialdehyde by the addition of H(2)O to the C-2, C-3 double bond, followed by the loss of HCl from the C-3 position. Sequence similarity between CaaD, an (alphabeta)(3) heterohexamer (molecular weight 47,547), and 4-oxalocrotonate tautomerase (4-OT), an (alpha)(6) homohexamer, distinguishes CaaD from those hydrolytic dehalogenases that form alkyl-enzyme intermediates. The recently solved X-ray structure of CaaD demonstrates that betaPro-1 (i.e., Pro-1 of the beta subunit), alphaArg-8, alphaArg-11, and alphaGlu-52 are at or near the active site, and the >or=10(3.4)-fold decreases in k(cat) on mutating these residues implicate them as mechanistically important. The effect of pH on k(cat)/K(m) indicates a catalytic base with a pK(a) of 7.6 and an acid with a pK(a) of 9.2. NMR titration of (15)N-labeled wild-type CaaD yielded pK(a) values of 9.3 and 11.1 for the N-terminal prolines, while the fully active but unstable alphaP1A mutant showed a pK(a) of 9.7 (for the betaPro-1), implicating betaPro-1 as the acid catalyst, which may protonate C-2 of the substrate. These results provide the first evidence for an amino-terminal proline, conserved in all known tautomerase superfamily members, functioning as a general acid, rather than as a general base as in 4-OT. Hence, a reasonable candidate for the general base in CaaD is the active site residue alphaGlu-52. CaaD has 10 arginine residues, six in the alpha-subunit (Arg-8, Arg-11, Arg-17, Arg-25, Arg-35, and Arg-43), and four in the beta-subunit (Arg-15, Arg-21, Arg-55, and Arg-65). (1)H-(15)N-heteronuclear single quantum coherence (HSQC) spectra of CaaD showed seven to nine Arg-NepsilonH resonances (denoted R(A) to R(I)) depending on the protein concentration and pH. One of these signals (R(D)) disappeared in the spectrum of the largely inactive alphaR11A mutant (deltaH = 7.11 ppm, deltaN = 89.5 ppm), and another one (R(G)) disappeared in the spectrum of the inactive alphaR8A mutant (deltaH = 7.48 ppm, deltaN = 89.6 ppm), thereby assigning these resonances to alphaArg-11NepsilonH, and alphaArg-8NepsilonH, respectively. (1)H-(15)N-HSQC titration of the enzyme with the substrate analogue 3-chloro-2-butenoic acid (3-CBA), a competitive inhibitor (K(I)(slope) = 0.35 +/- 0.06 mM), resulted in progressive downfield shifts of the alphaArg-8Nepsilon resonance yielding a K(D) = 0.77 +/- 0.44 mM, comparable to the (K(I)(slope), suggestive of active site binding. Increasing the pH of free CaaD to 8.9 at 5 degrees C resulted in the disappearance of all nine Arg-NepsilonH resonances due to base-catalyzed NepsilonH exchange. Saturating the enzyme with 3-CBA (16 mM) induced the reappearance of two NepsilonH signals, those of alphaArg-8 and alphaArg-11, indicating that the binding of the substrate analogue 3-CBA selectively slows the NepsilonH exchange rates of these two arginine residues. The kinetic and NMR data thus indicate that betaPro-1 is the acid catalyst, alphaGlu-52 is a reasonable candidate for the general base, and alphaArg-8 and alphaArg-11 participate in substrate binding and in stabilizing the aci-carboxylate intermediate in a Michael addition mechanism.
- Published
- 2004
20. Solution Structure and NH Exchange Studies of the MutT Pyrophosphohydrolase Complexed with Mg2+ and 8-Oxo-dGMP, a Tightly Bound Product
- Author
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Hugo F. Azurmendi, Albert S. Mildvan, V. Saraswat, and Michael A. Massiah
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Models, Molecular ,Molecular Sequence Data ,Guanosine Monophosphate ,Arginine ,Biochemistry ,Protein Structure, Secondary ,Substrate Specificity ,Adenosine Triphosphate ,Protein structure ,Escherichia coli ,Side chain ,Magnesium ,Amino Acid Sequence ,Pyrophosphatases ,Binding site ,Nuclear Magnetic Resonance, Biomolecular ,Binding Sites ,Chemistry ,Hydrogen bond ,Escherichia coli Proteins ,Deoxyguanine Nucleotides ,Hydrogen Bonding ,Phosphoric Monoester Hydrolases ,Recombinant Proteins ,Protein tertiary structure ,Protein Structure, Tertiary ,Solutions ,Crystallography ,Heteronuclear molecule ,Residual dipolar coupling ,Helix ,Nucleic Acid Conformation ,Protein Binding - Abstract
To learn the structural basis for the unusually tight binding of 8-oxo-nucleotides to the MutT pyrophosphohydrolase of Escherichia coli (129 residues), the solution structure of the MutT-Mg(2+)-8-oxo-dGMP product complex (K(D) = 52 nM) was determined by standard 3-D heteronuclear NMR methods. Using 1746 NOEs (13.5 NOEs/residue) and 186 phi and psi values derived from backbone (15)N, Calpha, Halpha, and Cbeta chemical shifts, 20 converged structures were computed with NOE violations
- Published
- 2003
21. Interactions of the Products, 8-Oxo-dGMP, dGMP, and Pyrophosphate with the MutT Nucleoside Triphosphate Pyrophosphohydrolase
- Author
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L. Mario Amzel, Albert S. Mildvan, Gregory Lopez, Michael A. Massiah, and V. Saraswat
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Cations, Divalent ,Macromolecular Substances ,Stereochemistry ,Guanosine Monophosphate ,Enzyme Activators ,Calorimetry ,Biochemistry ,Pyrophosphate ,Divalent ,chemistry.chemical_compound ,Non-competitive inhibition ,Magnesium ,heterocyclic compounds ,Nucleotide ,Enzyme Inhibitors ,Pyrophosphatases ,Nuclear Magnetic Resonance, Biomolecular ,chemistry.chemical_classification ,Manganese ,Nitrogen Isotopes ,Escherichia coli Proteins ,Temperature ,Deoxyguanine Nucleotides ,Phosphoric Monoester Hydrolases ,Diphosphates ,Enzyme Activation ,Kinetics ,Enzyme ,Models, Chemical ,chemistry ,Product inhibition ,Thermodynamics ,Protons ,Uncompetitive inhibitor ,Nucleoside - Abstract
The MutT enzyme from E. coli, in the presence of a divalent cation, catalyzes the hydrolysis of nucleoside- and deoxynucleoside-triphosphate (NTP) substrates by nucleophilic substitution at Pbeta, to yield a nucleotide (NMP) and PPi. The best substrate of MutT is believed to be the mutagenic nucleotide 8-oxo-dGTP, on the basis of its 10(3.4)-fold lower K(m) than that of dGTP (Maki, H., and Sekiguchi, M. (1992) Nature 355, 273-275). To determine the true affinity of MutT for an 8-oxo-nucleotide and to elucidate the kinetic scheme, product inhibition by 8-oxo-dGMP and dGMP and direct binding of these nucleotides to MutT were studied. With Mg(2+)-activated dGTP hydrolysis, 8-oxo-dGMP is a noncompetitive inhibitor with K(I)(sl)(o)(pe) = 49 nM, which is 10(4.6)-fold lower than the K(I)(sl)(o)(pe)of dGMP (1.7 mM). Similarly, the K(I)(intercept) of 8-oxo-dGMP is 10(4.0)-fold lower than that of dGMP. PPi is a linear uncompetitive inhibitor, suggesting that it dissociates first from the product complex, followed by the nucleotide. Noncompetitive inhibition by dGMP and 8-oxo-dGMP indicates an "iso" mechanism in which the nucleotide product leaves an altered form of the enzyme which slowly reverts to the form which binds substrate. Consistent with this kinetic scheme, (1)H-(15)N HSQC titration of MutT with dGMP reveals weak binding and fast exchange from one site with a K(D) = 1.8 mM, in agreement with its K(I)(sl)(o)(pe). With 8-oxo-dGMP, tight binding and slow exchange (n = 1.0 +/- 0.1, K(D)0.25 mM) are found. Isothermal calorimetric titration of MutT with 8-oxo-dGMP yields a K(D) of 52 nM, in agreement with its K(I)(sl)(o)(pe). Changing the metal activator from Mg(2+) to Mn(2+) had little effect on the K(I)(sl)(o)(pe) of dGMP or of 8-oxo-dGMP, consistent with the second-sphere enzyme-M(2+)-H(2)O-NTP-M(2+) complex found by NMR (Lin, J., Abeygunawardana, C., Frick, D. N., Bessman, M. J., and Mildvan, A. S. (1997) Biochemistry 36, 1199-1211), but it decreased the K(I) of PPi 12-fold, suggesting direct coordination of the PPi product by the enzyme-bound divalent cation. The tight binding of 8-oxo-dGMP to MutT (DeltaG degrees = -9.8 kcal/mol) is driven by a highly favorable enthalpy (DeltaH(binding)= -32 +/- 7 kcal/mol), with an unfavorable entropy (-TDeltaS(o)(binding)= +22 +/- 7 kcal/mol), as determined by van't Hoff analysis of the effect of temperature on the K(I)(sl)(o)(pe) and by isothermal titration calorimetry in two buffer systems. The binding of 8-oxo-dGMP to MutT induces changes in backbone (15)N and NH chemical shifts of 62 residues widely distributed throughout the protein, while dGMP binding induces smaller changes in only 22 residues surrounding the nucleotide binding site, suggesting that the unusually high affinity of MutT for 8-oxo-nucleotides is due not only to interactions with the altered 8-oxo or 7-NH positions on guanine, but results primarily from diffuse structural changes which tighten the protein structure around the 8-oxo-nucleotide.
- Published
- 2002
22. Short, strong hydrogen bonds on enzymes: NMR and mechanistic studies
- Author
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Putta Mallikarjuna Reddy, Albert S. Mildvan, Gregory T. Marks, David H. T. Harrison, Michael A. Massiah, Carol Viragh, Ildiko M. Kovach, and Thomas K. Harris
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Hydrogen bond ,Stereochemistry ,Chemical shift ,Organic Chemistry ,Isomerase ,Analytical Chemistry ,Triosephosphate isomerase ,Catalysis ,Inorganic Chemistry ,Serine ,chemistry.chemical_compound ,chemistry ,Ketosteroid ,Catalytic triad ,Spectroscopy - Abstract
The lengths of short, strong hydrogen bonds (SSHBs) on enzymes have been determined with high precision (±0.05 A) from the chemical shifts (δ), and independently from the D/H fractionation factors (φ) of the highly deshielded protons involved. These H-bond lengths agree well with each other and with those found by protein X-ray crystallography, within the larger errors of the latter method (±0.2 to±0.8 A) [Proteins 35 (1999) 275]. A model dihydroxynaphthalene compound shows a SSHB of 2.54±0.04 A based on δ=17.7 ppm and φ=0.56±0.04, in agreement with the high resolution X-ray distance of 2.55±0.06 A. On ketosteroid isomerase, a SSHB is found (2.50±0.02 A ), based on δ=18.2 ppm and φ=0.34, from Tyr-14 to the 3-O− of estradiol, an analog of the enolate intermediate. Its strength is ∼7 kcal/mol. On triosephosphate isomerase, SSHBs are found from Glu-165 to the 1-NOH of phosphoglycolohydroxamic acid (PGH), an analog of the enolic intermediate (2.55±0.05 A ), and from His-95 to the enolic-O− of PGH (2.62±0.02 A ). In the methylglyoxal synthase–PGH complex, a SSHB (2.51±0.02 A ) forms between Asp-71 and the NOH of PGH with a strength of ≥4.7 kcal/mol. When serine proteases bind mechanism-based inhibitors which form tetrahedral Ser-adducts analogous to the tetrahedral intermediates in catalysis, the Asp⋯His H-bond of the catalytic triad becomes a SSHB [Proc. Natl Acad. Sci. USA 95 (1998) 14664], 2.49–2.63 A in length. Similarly, on the serine-esterase, butyrylcholinesterase complexed with the mechanism-based inhibitor m-(N,N,N-trimethylammonio)-2,2,2-trifluoroacetophenone, a SSHB forms between Glu-327 and His-438 of the catalytic triad, 2.61±0.04 A in length, based on δ=18.1 ppm and φ=0.65±0.10. Very similar results are obtained with (human) acetylcholinesterase. The strength of this SSHB is at least 4.9 kcal/mol.
- Published
- 2002
23. Mutational, Kinetic, and NMR Studies of the Mechanism of E. coli GDP-Mannose Mannosyl Hydrolase, an Unusual Nudix Enzyme
- Author
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Albert S. Mildvan, Patricia M. Legler, and Michael A. Massiah
- Subjects
Glycoside Hydrolases ,Stereochemistry ,Glutamine ,DNA Mutational Analysis ,Molecular Sequence Data ,Glutamic Acid ,Arginine ,Biochemistry ,Catalysis ,Divalent ,Hydrolase ,Histidine ,Amino Acid Sequence ,Enzyme kinetics ,Pyrophosphatases ,Nuclear Magnetic Resonance, Biomolecular ,chemistry.chemical_classification ,biology ,Hydrogen bond ,Chemistry ,Escherichia coli Proteins ,Lysine ,Osmolar Concentration ,Temperature ,Leaving group ,Active site ,Hydrogen-Ion Concentration ,Dissociation constant ,Kinetics ,Amino Acid Substitution ,biology.protein ,Protons - Abstract
GDP-mannose mannosyl hydrolase (GDPMH) is an unusual Nudix family member, which catalyzes the hydrolysis of GDP-alpha-D-mannose to GDP and the beta-sugar by nucleophilic substitution at carbon rather than at phosphorus (Legler, P. M., Massiah, M. A., Bessman, M. J., and Mildvan, A. S. (2000) Biochemistry 39, 8603-8608). Using the structure and mechanism of MutT, the prototypical Nudix enzyme as a guide, we detected six catalytic residues of GDPMH, three of which were unique to GDPMH, by the kinetic and structural effects of site-specific mutations. Glu-70 (corresponding to Glu-57 in MutT) provides a ligand to the essential divalent cation on the basis of the effects of the E70Q mutation which decreased kcat 10(2.2)-fold, increased the dissociation constant of Mn2+ from the ternary E-Mn2+-GDP complex 3-fold, increased the K(m)Mg2+ 20-fold, and decreased the paramagnetic effect of Mn2+ on 1/T1 of water protons, indicating a change in the coordination sphere of Mn2+. In the E70Q mutant, Gln-70 was shown to be very near the active site metal ion by large paramagnetic effects of Mn2+ on its side chain -NH2 group. With wild-type GDPMH, the effect of pH on log(kcat/K(m)GDPmann) at 37 degrees C showed an ascending limb of unit slope, followed by a plateau yielding a pK(a) of 6.4, which increased to 6.7 +/- 0.1 in the pH dependence of log(kcat). The general base catalyst was identified as a neutral His residue by the DeltaH(ionization) = 7.0 +/- 0.7 kcal/mol, by the increase in pK(a) with ionic strength, and by mutation of each of the four histidine residues of GDPMH to Gln. Only the H124Q mutant showed the loss of the ascending limb in the pH versus log(kcat) rate profile, which was replaced by a weak dependence of rate on hydroxide concentration, as well as an overall 10(3.4)-fold decrease in kcat, indicating His-124 to be the general base, unlike MutT, which uses Glu-53 in this role. The H88Q mutant showed a 10(2.3)-fold decrease in kcat, a 4.4-fold increase in K(m)GDPmann, and no change in the pH versus log(kcat) rate profile, indicating an important but unidentified role of His-88 in catalysis. One and two-dimensional NMR studies permitted the sequence specific assignments of the imidazole HdeltaC, H(epsilon)C, N(delta), and N(epsilon) resonances of the four histidines and defined their protonation states. The pK(a) of His-124 (6.94 +/- 0.04) in the presence of saturating Mg2+ was comparable to the kinetically determined pK(a) at the same temperature (6.40 +/- 0.20). The other three histidines were neutral N(epsilon)H tautomers with pK(a) values below 5.5. Arg-52 and Arg-65 were identified as catalytic residues which interact electrostatically with the GDP leaving group by mutating these residues to Gln and Lys. The R52Q mutant decreased kcat 309-fold and increased K(m)GDPmann 40.6-fold, while the R52K mutant decreased kcat by only 12-fold and increased K(m)GDPmann 81-fold. The partial rescue of kcat, but not of K(m)GDPmann in the R52K mutant, suggests that Arg-52 is a bifunctional hydrogen bond donor to the GDP leaving group in the ground state and a monofunctional hydrogen bond donor in the transition state. Opposite behavior was found with the Arg-65 mutants, suggesting this residue to be a monofunctional hydrogen bond donor to the GDP leaving group in the ground state and a bifunctional hydrogen bond donor in the transition state. From these observations, a mechanism for GDPMH is proposed involving general base catalysis and electrostatic stabilization of the leaving group.
- Published
- 2002
24. MID1 catalyzes the ubiquitination of protein phosphatase 2A and mutations within its Bbox1 domain disrupt polyubiquitination of alpha4 but not of PP2Ac
- Author
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Alma Didoronkute, Marcus V. A. Levy, Haijuan Du, Nimish Todi, Michael A. Massiah, Anna Shchelokova, and Kuanlin Wu
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Models, Molecular ,medicine.disease_cause ,Biochemistry ,Protein structure ,Protein Phosphatase 2 ,Hypospadias ,0303 health sciences ,Mutation ,Multidisciplinary ,Hypertelorism ,biology ,030302 biochemistry & molecular biology ,Intracellular Signaling Peptides and Proteins ,Nuclear Proteins ,Signal transducing adaptor protein ,Genetic Diseases, X-Linked ,3. Good health ,Ubiquitin ligase ,Cleft Palate ,embryonic structures ,Microtubule Proteins ,Medicine ,Research Article ,Signal Transduction ,Recombinant Fusion Proteins ,Ubiquitin-Protein Ligases ,Protein subunit ,Science ,Molecular Sequence Data ,Protein Chemistry ,03 medical and health sciences ,Esophagus ,Chemical Biology ,medicine ,Humans ,Amino Acid Sequence ,Adaptor Proteins, Signal Transducing ,030304 developmental biology ,Sequence Homology, Amino Acid ,Point mutation ,Ubiquitination ,Biology and Life Sciences ,Proteins ,Protein phosphatase 2 ,Fibroblasts ,Biochemical Activity ,Protein Structure, Tertiary ,Gene Expression Regulation ,Biocatalysis ,Enzymology ,biology.protein ,Sequence Alignment ,TRIM Family ,Developmental Biology ,Molecular Chaperones ,Transcription Factors - Abstract
MID1 is a microtubule-associated protein that belongs to the TRIM family. MID1 functions as an ubiquitin E3 ligase, and recently was shown to catalyze the polyubiquitination of, alpha4, a protein regulator of protein phosphatase 2A (PP2A). It has been hypothesized that MID1 regulates PP2A, requiring the intermediary interaction with alpha4. Here we report that MID1 catalyzes the in vitro ubiquitination of the catalytic subunit of PP2A (PP2Ac) in the absence of alpha4. In the presence of alpha4, the level of PP2Ac ubiquitination is reduced. Using the MID1 RING-Bbox1-Bbox2 (RB1B2) construct containing the E3 ligase domains, we investigate the functional effects of mutations within the Bbox domains that are identified in patients with X-linked Opitz G syndrome (XLOS). The RB1B2 proteins harboring the C142S, C145T, A130V/T mutations within the Bbox1 domain and C195F mutation within the Bbox2 domain maintain auto-polyubiquitination activity. Qualitatively, the RB1B2 proteins containing these mutations are able to catalyze the ubiquitination of PP2Ac. In contrast, the RB1B2 proteins with mutations within the Bbox1 domain are unable to catalyze the polyubiquitination of alpha4. These results suggest that unregulated alpha4 may be the direct consequence of these natural mutations in the Bbox1 domain of MID1, and hence alpha4 could play a greater role to account for the increased amount of PP2A observed in XLOS-derived fibroblasts.
- Published
- 2014
25. Potency of Michael reaction acceptors as inducers of enzymes that protect against carcinogenesis depends on their reactivity with sulfhydryl groups
- Author
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Ronald J. Hicks, Paul Talalay, Albena T. Dinkova-Kostova, Richard E. Bozak, and Michael A. Massiah
- Subjects
Carcinoma, Hepatocellular ,Magnetic Resonance Spectroscopy ,FMN Reductase ,Stereochemistry ,Substituent ,Cyclopentanes ,Alkylation ,Benzylidene Compounds ,Mice ,chemistry.chemical_compound ,Chalcone ,Nucleophile ,Coumarins ,Tumor Cells, Cultured ,Animals ,Humans ,NADH, NADPH Oxidoreductases ,Inducer ,Sulfhydryl Compounds ,Enzyme inducer ,Glutathione Transferase ,Multidisciplinary ,Molecular Structure ,biology ,Cyclohexanones ,Liver Neoplasms ,Glutathione ,Biological Sciences ,Butanones ,chemistry ,Cinnamates ,Enzyme Induction ,Electrophile ,Commentary ,biology.protein ,Michael reaction - Abstract
Induction of phase 2 enzymes and elevations of glutathione are major and sufficient strategies for protecting mammals and their cells against the toxic and carcinogenic effects of electrophiles and reactive forms of oxygen. Inducers belong to nine chemical classes and have few common properties except for their ability to modify sulfhydryl groups by oxidation, reduction, or alkylation. Much evidence suggests that the cellular “sensor” molecule that recognizes the inducers and signals the enhanced transcription of phase 2 genes does so by virtue of unique and highly reactive sulfhydryl functions that recognize and covalently react with the inducers. Benzylidene-alkanones and -cycloalkanones are Michael reaction acceptors whose inducer potency is profoundly increased by the presence of ortho- (but not other) hydroxyl substituent(s) on the aromatic ring(s). This enhancement correlates with more rapid reactivity of the ortho -hydroxylated derivatives with model sulfhydryl compounds. Proton NMR spectroscopy provides no evidence for increased electrophilicity of the β-vinyl carbons (the presumed site of nucleophilic attack) on the hydroxylated inducers. Surprisingly, these ortho -hydroxyl groups display a propensity for extensive intermolecular hydrogen bond formation, which may raise the reactivity and facilitate addition of mercaptans, thereby raising inducer potencies.
- Published
- 2001
26. NMR Evidence for a Short, Strong Hydrogen Bond at the Active Site of a Cholinesterase
- Author
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Albert S. Mildvan, Michael A. Massiah, Thomas K. Harris, Putta Mallikarjuna Reddy, Ildiko M. Kovach, and Carol Viragh
- Subjects
Proteases ,Stereochemistry ,Biochemistry ,Paraoxon ,Catalysis ,Serine ,Nucleophile ,Catalytic triad ,Animals ,Organic chemistry ,Horses ,Nuclear Magnetic Resonance, Biomolecular ,Cholinesterase ,Binding Sites ,integumentary system ,biology ,Chemistry ,Hydrogen bond ,Acetophenones ,Active site ,Hydrogen Bonding ,Enzyme Activation ,Kinetics ,Butyrylcholinesterase ,biology.protein ,Cholinesterase Inhibitors - Abstract
Cholinesterases (ChE), use a Glu-His-Ser catalytic triad to enhance the nucleophilicity of the catalytic serine. It has been shown that serine proteases, which employ an Asp-His-Ser catalytic triad for optimal catalytic efficiency, decrease the hydrogen bonding distance between the Asp-His pair to form a short, strong hydrogen bond (SSHB) upon binding mechanism-based inhibitors, which form tetrahedral Ser-adducts, analogous to the tetrahedral intermediates in catalysis, or at low pH when the histidine is protonated [Cassidy, C. S., Lin, J., Frey, P. A. (1997) Biochemistry 36, 4576-4584]. Two types of mechanism-based inhibitors were bound to pure equine butyrylcholinesterase (BChE), a 364 kDa homotetramer, and the complexes were studied by (1)H NMR at 600 MHz and 25-37 degrees C. The downfield region of the (1)H NMR spectrum of free BChE at pH 7.5 showed a broad, weak, deshielded resonance with a chemical shift, delta = 16.1 ppm, ascribed to a small amount of the histidine-protonated form. Upon addition of a 3-fold excess of diethyl 4-nitrophenyl phosphate (paraoxon) and subsequent dealkylation, the broad 16.1 ppm resonance increased in intensity 4.7-fold, and yielded a D/H fractionation factor phi = 0.72+/-0.10 consistent with a SSHB between Glu and His of the catalytic triad. From an empirical correlation of delta with hydrogen-bond length in small crystalline compounds, the length of this SSBH is 2.64+/-0.04 A, in agreement with the length of 2.62+/-0.02 A independently obtained from phi. The addition of a 3-fold excess of m-(N,N, N-trimethylammonio)trifluoroacetophenone to BChE yielded no signal at 16.1 ppm, and a 640 Hz broad, highly deshielded proton resonance with a chemical shift delta = 18.1 ppm and a D/H fractionation factor phi = 0.63+/-0.10, also consistent with a SSHB. The length of this SSHB is calculated to be 2.62+/-0.04 A from delta and 2.59+/-0.03 A from phi. These NMR-derived distances agree with those found in the X-ray structures of the homologous acetylcholinesterase complexed with the same mechanism-based inhibitors, 2.60+/-0.22 and 2.66+/-0.28 A. However, the order of magnitude greater precision of the NMR-derived distances establish the presence of SSHBs. We suggest that ChEs achieve their remarkable catalytic power in ester hydrolysis, in part, due to the formation of a SSHB between Glu and His of the catalytic triad.
- Published
- 2000
27. GDP-Mannose Mannosyl Hydrolase Catalyzes Nucleophilic Substitution at Carbon, Unlike All Other Nudix Hydrolases
- Author
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Maurice J. Bessman, Patricia M. Legler, Michael A. Massiah, and Albert S. Mildvan
- Subjects
Magnetic Resonance Spectroscopy ,Glycoside Hydrolases ,Stereochemistry ,Chemistry ,Escherichia coli Proteins ,Mannose ,medicine.disease_cause ,Nudix hydrolases ,Guanosine Diphosphate ,Biochemistry ,Carbon ,Substrate Specificity ,Molecular Weight ,Kinetics ,Hydrolysis ,chemistry.chemical_compound ,Models, Chemical ,Hydrolase ,Escherichia coli ,medicine ,Nucleophilic substitution ,Protein Structure, Quaternary ,Dimerization - Abstract
GDP-mannose mannosyl hydrolase (GDPMH) from Escherichia coli is a 36. 8 kDa homodimer which, in the presence of Mg(2+), catalyzes the hydrolysis of GDP-alpha-D-mannose or GDP-alpha-D-glucose to yield sugar and GDP. On the basis of its amino acid sequence, GDPMH is a member of the Nudix family of enzymes which catalyze the hydrolysis of nucleoside diphosphate derivatives by nucleophilic substitution at phosphorus. However, GDPMH has a sequence rearrangement (RE to ER) in the conserved Nudix motif and is missing a Glu residue characteristic of the Nudix signature sequence. By (1)H NMR, the initial hydrolysis product of GDP-alpha-D-glucose is beta-D-glucose, indicating nucleophilic substitution with inversion at C1' of glucose. Substitution at carbon was confirmed by two-dimensional (1)H-(13)C HSQC spectra of the products of hydrolysis in 48.4% (18)O-labeled water which showed an additional C1' resonance of beta-D-glucose with a typical upfield (18)O isotope shift of 18 ppb and an intensity of 47.6% of the total signal. No (18)O isotope-shifted resonances (4%) were found in the (31)P NMR spectrum of the GDP product. Thus, unlike all other Nudix enzymes studied so far, GDPMH catalyzes nucleophilic substitution at carbon rather than at phosphorus. A small solvent kinetic deuterium isotope effect on k(cat) of 1.76 +/- 0.25, independent of pH over the range of 6.0-9.3, suggests that the deprotonation of water may be part of the rate-limiting step.
- Published
- 2000
28. Mutational, Kinetic, and NMR Studies of the Roles of Conserved Glutamate Residues and of Lysine-39 in the Mechanism of the MutT Pyrophosphohydrolase
- Author
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Albert S. Mildvan, Gong Wu, Michael A. Massiah, and Thomas K. Harris
- Subjects
Protein Conformation ,Stereochemistry ,Glutamine ,DNA Mutational Analysis ,Mutant ,Magnesium Chloride ,Glutamic Acid ,Binding, Competitive ,Biochemistry ,Catalysis ,Divalent ,Adenosine Triphosphate ,Bacterial Proteins ,Chlorides ,Magnesium ,Nucleotide ,Pyrophosphatases ,Binding site ,Nuclear Magnetic Resonance, Biomolecular ,Conserved Sequence ,chemistry.chemical_classification ,Aspartic Acid ,Manganese ,Nitrogen Isotopes ,biology ,Chemistry ,Ligand ,Escherichia coli Proteins ,Lysine ,Wild type ,Active site ,Phosphoric Monoester Hydrolases ,Recombinant Proteins ,Protein Structure, Tertiary ,Kinetics ,Manganese Compounds ,Mutagenesis, Site-Directed ,Solvents ,biology.protein ,Protons ,Heteronuclear single quantum coherence spectroscopy ,Protein Binding - Abstract
The MutT enzyme catalyzes the hydrolysis of nucleoside triphosphates (NTP) to NMP and PP(i) by nucleophilic substitution at the rarely attacked beta-phosphorus. The solution structure of the quaternary E-M(2+)-AMPCPP-M(2+) complex indicated that conserved residues Glu-53, -56, -57, and -98 are at the active site near the bound divalent cation possibly serving as metal ligands, Lys-39 is positioned to promote departure of the NMP leaving group, and Glu-44 precedes helix I (residues 47-59) possibly stabilizing this helix which contributes four catalytic residues to the active site [Lin, J. , Abeygunawardana, C., Frick, D. N., Bessman, M. J., and Mildvan, A. S. (1997) Biochemistry 36, 1199-1211]. To test these proposed roles, the effects of mutations of each of these residues on the kinetic parameters and on the Mn(2+), Mg(2+), and substrate binding properties were examined. The largest decreases in k(cat) for the Mg(2+)-activated enzyme of 10(4.7)- and 10(2.6)-fold were observed for the E53Q and E53D mutants, respectively, while 97-, 48-, 25-, and 14-fold decreases were observed for the E44D, E56D, E56Q, and E44Q mutations, respectively. Smaller effects on k(cat) were observed for mutations of Glu-98 and Lys-39. For wild type MutT and its E53D and E44D mutants, plots of log(k(cat)) versus pH exhibited a limiting slope of 1 on the ascending limb and then a hump, i.e., a sharply defined maximum near pH 8 followed by a plateau, yielding apparent pK(a) values of 7.6 +/- 0.3 and 8.4 +/- 0.4 for an essential base and a nonessential acid catalyst, respectively, in the active quaternary MutT-Mg(2+)-dGTP-Mg(2+) complex. The pK(a) of 7.6 is assigned to Glu-53, functioning as a base catalyst in the active quaternary complex, on the basis of the disappearance of the ascending limb of the pH-rate profile of the E53Q mutant, and its restoration in the E53D mutant with a 10(1.9)-fold increase in (k(cat))(max). The pK(a) of 8.4 is assigned to Lys-39 on the basis of the disappearance of the descending limb of the pH-rate profile of the K39Q mutant, and the observation that removal of the positive charge of Lys-39, by either deprotonation or mutation, results in the same 8.7-fold decrease in k(cat). Values of k(cat) of both wild type MutT and the E53Q mutant were independent of solvent viscosity, indicating that a chemical step is likely to be rate-limiting with both. A liganding role for Glu-53 and Glu-56, but not Glu-98, in the binary E-M(2+) complex is indicated by the observation that the E53Q, E53D, E56Q, and E56D mutants bound Mn(2+) at the active site 36-, 27-, 4.7-, and 1.9-fold weaker, and exhibited 2.10-, 1.50-, 1.12-, and 1.24-fold lower enhanced paramagnetic effects of Mn(2+), respectively, than the wild type enzyme as detected by 1/T(1) values of water protons, consistent with the loss of a metal ligand. However, the K(m) values of Mg(2+) and Mn(2+) indicate that Glu-56, and to a lesser degree Glu-98, contribute to metal binding in the active quaternary complex. Mutations of the more distant but conserved residue Glu-44 had little effect on metal binding or enhancement factors in the binary E-M(2+) complexes. Two-dimensional (1)H-(15)N HSQC and three-dimensional (1)H-(15)N NOESY-HSQC spectra of the kinetically damaged E53Q and E56Q mutants showed largely intact proteins with structural changes near the mutated residues. Structural changes in the kinetically more damaged E44D mutant detected in (1)H-(15)N HSQC spectra were largely limited to the loop I-helix I motif, suggesting that Glu-44 stabilizes the active site region. (1)H-(15)N HSQC titrations of the E53Q, E56Q, and E44D mutants with dGTP showed changes in chemical shifts of residues lining the active site cleft, and revealed tighter nucleotide binding by these mutants, indicating an intact substrate binding site. (ABSTRACT TRUNCATED)
- Published
- 2000
29. Kinetic, Stereochemical, and Structural Effects of Mutations of the Active Site Arginine Residues in 4-Oxalocrotonate Tautomerase
- Author
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Christian P. Whitman, Robert M. Czerwinski, Albert S. Mildvan, James T. Stivers, Michael A. Massiah, Patricia M. Legler, Thomas K. Harris, Chitrananda Abeygunawardana, and William H. Johnson
- Subjects
Models, Molecular ,Stereochemistry ,Glutamine ,Protonation ,Arginine ,Biochemistry ,Catalysis ,Enzyme kinetics ,Isomerases ,Nuclear Magnetic Resonance, Biomolecular ,Alanine ,Binding Sites ,Nitrogen Isotopes ,biology ,Pseudomonas putida ,Chemistry ,Mutagenesis ,Titrimetry ,Active site ,Substrate (chemistry) ,Cooperative binding ,Stereoisomerism ,Recombinant Proteins ,Sorbic Acid ,Kinetics ,Mutagenesis, Site-Directed ,biology.protein ,4-Oxalocrotonate tautomerase ,Stereoselectivity - Abstract
Three arginine residues (Arg-11, Arg-39, Arg-61) are found at the active site of 4-oxalocrotonate tautomerase in the X-ray structure of the affinity-labeled enzyme [Taylor, A. B., Czerwinski, R. M., Johnson, R. M., Jr., Whitman, C. P., and Hackert, M. L. (1998) Biochemistry 37, 14692-14700]. The catalytic roles of these arginines were examined by mutagenesis, kinetic, and heteronuclear NMR studies. With a 1,6-dicarboxylate substrate (2-hydroxymuconate), the R61A mutation showed no kinetic effects, while the R11A mutation decreased k(cat) 88-fold and increased K(m) 8.6-fold, suggesting both binding and catalytic roles for Arg-11. With a 1-monocarboxylate substrate (2-hydroxy-2,4-pentadienoate), no kinetic effects of the R11A mutation were found, indicating that Arg-11 interacts with the 6-carboxylate of the substrate. The stereoselectivity of the R11A-catalyzed protonation at C-5 of the dicarboxylate substrate decreased, while the stereoselectivity of protonation at C-3 of the monocarboxylate substrate increased in comparison with wild-type 4-OT, indicating the importance of Arg-11 in properly orienting the dicarboxylate substrate by interacting with the charged 6-carboxylate group. With 2-hydroxymuconate, the R39A and R39Q mutations decreased k(cat) by 125- and 389-fold and increased K(m) by 1.5- and 2.6-fold, respectively, suggesting a largely catalytic role for Arg-39. The activity of the R11A/R39A double mutant was at least 10(4)-fold lower than that of the wild-type enzyme, indicating approximate additivity of the effects of the two arginine mutants on k(cat). For both R11A and R39Q, 2D (1)H-(15)N HSQC and 3D (1)H-(15)N NOESY-HSQC spectra showed chemical shift changes mainly near the mutated residues, indicating otherwise intact protein structures. The changes in the R39Q mutant were mainly in the beta-hairpin from residues 50 to 57 which covers the active site. HSQC titration of R11A with the substrate analogue cis, cis-muconate yielded a K(d) of 22 mM, 37-fold greater than the K(d) found with wild-type 4-OT (0.6 mM). With the R39Q mutant, cis, cis-muconate showed negative cooperativity in active site binding with two K(d) values, 3.5 and 29 mM. This observation together with the low K(m) of 2-hydroxymuconate (0.47 mM) suggests that only the tight binding sites function catalytically in the R39Q mutant. The (15)Nepsilon resonances of all six Arg residues of 4-OT were assigned, and the assignments of Arg-11, -39, and -61 were confirmed by mutagenesis. The binding of cis,cis-muconate to wild-type 4-OT upshifts Arg-11 Nepsilon (by 0.05 ppm) and downshifts Arg-39 Nepsilon (by 1.19 ppm), indicating differing electronic delocalizations in the guanidinium groups. A mechanism is proposed in which Arg-11 interacts with the 6-carboxylate of the substrate to facilitate both substrate binding and catalysis and Arg-39 interacts with the 1-carboxylate and the 2-keto group of the substrate to promote carbonyl polarization and catalysis, while Pro-1 transfers protons from C-3 to C-5. This mechanism, together with the effects of mutations of catalytic residues on k(cat), provides a quantitative explanation of the 10(7)-fold catalytic power of 4-OT. Despite its presence in the active site in the crystal structure of the affinity-labeled enzyme, Arg-61 does not play a significant role in either substrate binding or catalysis.
- Published
- 1999
30. Cystic Fibrosis Transmembrane Conductance Regulator: Solution Structures of Peptides Based on the Phe508 Region, the Most Common Site of Disease-Causing ΔF508 Mutation
- Author
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Albert S. Mildvan, Peter L. Pedersen, Young Hee Ko, and Michael A. Massiah
- Subjects
Models, Molecular ,Stereochemistry ,Phenylalanine ,Molecular Sequence Data ,Cystic Fibrosis Transmembrane Conductance Regulator ,Peptide ,medicine.disease_cause ,Biochemistry ,Cystic fibrosis ,Protein Structure, Secondary ,Residue (chemistry) ,medicine ,Humans ,Point Mutation ,Dimethyl Sulfoxide ,Amino Acid Sequence ,Mathematical Computing ,Nuclear Magnetic Resonance, Biomolecular ,chemistry.chemical_classification ,Mutation ,biology ,Chemical shift ,Water ,Trifluoroethanol ,medicine.disease ,Peptide Fragments ,Cystic fibrosis transmembrane conductance regulator ,Solutions ,chemistry ,Helix ,Proton NMR ,biology.protein - Abstract
Most cases of cystic fibrosis (CF), a common inherited disease of epithelial cell origin, are caused by the deletion of Phe508 located in the first nucleotide-binding domain (NBF1) of the protein called CFTR (cystic fibrosis transmembrane conductance regulator). To gain greater insight into the structure within the Phe508 region of the wild-type protein and the change in structure that occurs when this residue is deleted, we conducted nuclear magnetic resonance (NMR) studies on representative synthetic 26 and 25 amino acid peptide segments. 2D 1H NMR studies at 600 MHz of the 26-residue peptide consisting of Met498 to Ala523 in 10% DMSO, pH 4.0, at 25 degrees C show a continuous but labile helix from Gly500 to Lys522, based on both NH-NH(i,i+1) and alphaH-NH(i,i+1) NOEs. Phe508 within this helix shows only short-range (i
- Published
- 1999
31. Three-Dimensional Structure of the HTLV-II Matrix Protein and Comparative Analysis of Matrix Proteins from the Different Classes of Pathogenic Human Retroviruses
- Author
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Allyson M. Christensen, Brian G. Turner, Michael A. Massiah, Wesley I. Sundquist, and Michael F. Summers
- Subjects
Models, Molecular ,Magnetic Resonance Spectroscopy ,Protein Conformation ,Molecular Sequence Data ,Matrix (biology) ,Biology ,Protein Structure, Secondary ,Viral Matrix Proteins ,Species Specificity ,Structural Biology ,310 helix ,Escherichia coli ,Humans ,Amino Acid Sequence ,Molecular Biology ,Integral membrane protein ,Myristoylation ,Human T-lymphotropic virus 1 ,Viral matrix protein ,Sequence Homology, Amino Acid ,C-terminus ,Human T-lymphotropic virus 2 ,Viral membrane ,Recombinant Proteins ,Protein Structure, Tertiary ,Crystallography ,Retroviridae ,HIV-1 ,Biophysics ,Oncovirus - Abstract
The matrix protein performs similar roles in all retroviruses, initially directing membrane localization of the assembling viral particle and subsequently forming a stable structural shell associated with the inner surface of the mature viral membrane. Although conserved structural elements are likely to perform these functions in all retroviral matrix proteins, invariant motifs are not evident at the primary sequence level and three-dimensional structures have been available for only the primate lentiviral matrix proteins. We have therefore used NMR spectroscopy to determine the structure of the matrix protein from human T-cell leukemia virus type II (HTLV-II), a member of the human oncovirus subclass of retroviruses. A total of 577 distance restraints were used to build 20 refined models that superimpose with an rmsd of 0.71 A for the backbone atoms of the structured regions. The globular HTLV-II matrix structure is composed of four α-helices and a 3 10 helix. Exposed basic residues near the C terminus of helix II form a putative membrane binding surface which could act in concert with the N-terminal myristoyl group to anchor the protein on the viral membrane surface. Clear structural similarities between the HTLV-II and HIV-1 matrix proteins suggest that the topology and exposed cationic membrane binding surface are likely to be conserved features of retroviral matrix proteins.
- Published
- 1996
32. NMR Studies of the C-Terminus of alpha4 Reveal Possible Mechanism of Its Interaction with MID1 and Protein Phosphatase 2A
- Author
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Michael A. Massiah and Haijuan Du
- Subjects
Proteomics ,Models, Molecular ,Protein Folding ,Magnetic Resonance Spectroscopy ,lcsh:Medicine ,Plasma protein binding ,Biochemistry ,Physical Chemistry ,Protein Structure, Secondary ,0302 clinical medicine ,Protein structure ,Macromolecular Structure Analysis ,Protein Phosphatase 2 ,Biomacromolecule-Ligand Interactions ,lcsh:Science ,Micelles ,0303 health sciences ,Multidisciplinary ,biology ,Chemistry ,Applied Chemistry ,Intracellular Signaling Peptides and Proteins ,Sodium Dodecyl Sulfate ,Ubiquitin ligase ,Solutions ,030220 oncology & carcinogenesis ,Microtubule Proteins ,Research Article ,Protein Binding ,Protein Structure ,Protein subunit ,Nuclear Magnetic Resonance ,Phosphatase ,Molecular Sequence Data ,Static Electricity ,Biophysics ,Protein Chemistry ,Chemical shift index ,03 medical and health sciences ,Humans ,Amino Acid Sequence ,Protein Interactions ,Biology ,030304 developmental biology ,Adaptor Proteins, Signal Transducing ,C-terminus ,lcsh:R ,Proteins ,Computational Biology ,Protein phosphatase 2 ,Protein Structure, Tertiary ,Chemical Properties ,biology.protein ,lcsh:Q ,Molecular Chaperones - Abstract
Alpha4 is a regulatory subunit of the protein phosphatase family of enzymes and plays an essential role in regulating the catalytic subunit of PP2A (PP2Ac) within the rapamycin-sensitive signaling pathway. Alpha4 also interacts with MID1, a microtubule-associated ubiquitin E3 ligase that appears to regulate the function of PP2A. The C-terminal region of alpha4 plays a key role in the binding interaction of PP2Ac and MID1. Here we report on the solution structure of a 45-amino acid region derived from the C-terminus of alpha4 (alpha45) that binds tightly to MID1. In aqueous solution, alpha45 has properties of an intrinsically unstructured peptide although chemical shift index and dihedral angle estimation based on chemical shifts of backbone atoms indicate the presence of a transient α-helix. Alpha45 adopts a helix-turn-helix HEAT-like structure in 1% SDS micelles, which may mimic a negatively charged surface for which alpha45 could bind. Alpha45 binds tightly to the Bbox1 domain of MID1 in aqueous solution and adopts a structure consistent with the helix-turn-helix structure observed in 1% SDS. The structure of alpha45 reveals two distinct surfaces, one that can interact with a negatively charged surface, which is present on PP2A, and one that interacts with the Bbox1 domain of MID1.
- Published
- 2011
33. Detection and characterization of the in vitro e3 ligase activity of the human MID1 protein
- Author
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Michael A. Massiah, Xiaofeng Han, and Haijuan Du
- Subjects
Models, Molecular ,Protein subunit ,Ubiquitin-Protein Ligases ,Mutant ,Molecular Sequence Data ,Peptide ,Biology ,Models, Biological ,Protein structure ,Ubiquitin ,Structural Biology ,Humans ,Amino Acid Sequence ,Molecular Biology ,Peptide sequence ,chemistry.chemical_classification ,Ubiquitination ,Nuclear Proteins ,Protein phosphatase 2 ,Ubiquitin ligase ,Protein Structure, Tertiary ,Biochemistry ,chemistry ,biology.protein ,Microtubule Proteins ,Transcription Factors - Abstract
Human MID1 (midline-1) is a microtubule-associated protein that is postulated to target the catalytic subunit of protein phosphatase 2A for degradation. It binds alpha4 that then recruits the catalytic subunit of protein phosphatase 2A. As a member of the TRIM (tripartite motif) family, MID1 has three consecutive zinc-binding domains-RING (really interesting new gene), Bbox1, and Bbox2-that have similar ββα-folds. Here, we describe the in vitro characterization of these domains individually and in tandem. We observed that the RING domain exhibited greater ubiquitin (Ub) E3 ligase activity compared to the Bbox domains. The amount of autopolyubiquitinated products with RING-Bbox1 and RING-Bbox1-Bbox2 domains in tandem was significantly greater than those of the individual domains. However, no polyubiquitinated products were observed for the Bbox1-Bbox domains in tandem. Using mutants of Ub, we observed that these MID1 domain constructs facilitate Ub chain elongation via Lys63 of Ub. In addition, we observed that the high-molecular-weight protein products were primarily due to polyubiquitination at one site (Lys154) on the Bbox1 domain of the RING-Bbox1 and RING-Bbox1-Bbox2 constructs. We observed that MID1 E3 domains could interact with multiple E2-conjugating enzymes. Lastly, a 45-amino-acid peptide derived from the C-terminus of alpha4 that binds tightly to Bbox1 was observed to be monoubiquitinated in the assay and appears to down-regulate the amount of polyubiquitinated products formed. These studies shed light on MID1 E3 ligase activity and show how its three zinc-binding domains can contribute to MID1's overall function.
- Published
- 2010
34. Solution structure of the MID1 B-box2 CHC(D/C)C(2)H(2) zinc-binding domain: insights into an evolutionarily conserved RING fold
- Author
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Suryaparkash Singireddy, Timothy C. Cox, Michael A. Massiah, Zou Yi, Jessica Matts, Brandi Simmons, and Kieran M. Short
- Subjects
Models, Molecular ,Protein Folding ,Magnetic Resonance Spectroscopy ,EGF-like domain ,Ubiquitin-Protein Ligases ,Protein domain ,Molecular Sequence Data ,Evolution, Molecular ,Protein structure ,Structural Biology ,EVH1 domain ,Humans ,Amino Acid Sequence ,Molecular Biology ,Conserved Sequence ,Zinc finger ,Chemistry ,Nuclear Proteins ,Zinc Fingers ,Phosphoproteins ,Protein tertiary structure ,Protein Structure, Tertiary ,Solutions ,Crystallography ,Zinc ,Cyclic nucleotide-binding domain ,Microtubule Proteins ,Protein folding ,Transcription Factors - Abstract
The B-box type 2 domain is a prominent feature of a large and growing family of RING, B-box, coiled-coil (RBCC) domain-containing proteins and is also present in more than 1500 additional proteins. Most proteins usually contain a single B-box2 domain, although some proteins contain tandem domains consisting of both type 1 and type 2 B-boxes, which actually share little sequence similarity. Recently, we determined the solution structure of B-box1 from MID1, a putative E3 ubiquitin ligase that is mutated in X-linked Opitz G/BBB syndrome, and showed that it adopted a betabetaalpha RING-like fold. Here, we report the tertiary structure of the B-box2 (CHC(D/C)C(2)H(2)) domain from MID1 using multidimensional NMR spectroscopy. This MID1 B-box2 domain consists of a short alpha-helix and a structured loop with two short anti-parallel beta-strands and adopts a tertiary structure similar to the B-box1 and RING structures, even though there is minimal primary sequence similarity between these domains. By mutagenesis, ESI-FTICR and ICP mass spectrometry, we show that the B-box2 domain coordinates two zinc atoms with a 'cross-brace' pattern: one by Cys175, His178, Cys195 and Cys198 and the other by Cys187, Asp190, His204, and His207. Interestingly, this is the first case that an aspartic acid is involved in zinc atom coordination in a zinc-finger domain, although aspartic acid has been shown to coordinate non-catalytic zinc in matrix metalloproteinases. In addition, the finding of a Cys195Phe substitution identified in a patient with X-linked Opitz GBBB syndrome supports the importance of proper zinc coordination for the function of the MID1 B-box2 domain. Notably, however, our structure differs from the only other published B-box2 structure, that from XNF7, which was shown to coordinate one zinc atom. Finally, the similarity in tertiary structures of the B-box2, B-box1 and RING domains suggests these domains have evolved from a common ancestor.
- Published
- 2007
35. Membrane Interactions with NA-CATH
- Author
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Susan D. Gillmor, Barney Bishop, Michael A. Massiah, Robin Samuel, and Haijuad Du
- Subjects
Phosphatidylglycerol ,chemistry.chemical_classification ,Liposome ,Biophysics ,Biology ,Fluorescence ,Amino acid ,chemistry.chemical_compound ,Membrane ,chemistry ,Biochemistry ,Amphiphile ,Cardiolipin ,Cationic Antimicrobial Peptides ,lipids (amino acids, peptides, and proteins) - Abstract
The “catastrophic threat” of antibiotic resistance has prompted research into biological methods of combating bacterial infection. One such pervasive strategy employs cationic antimicrobial peptides, CAMPs. These peptides use their structure to target and disrupt bacterial membranes. They specifically attach to PG (phosphatidylglycerol) and CL (cardiolipin) rich membranes, a common, anionic lipid of the outer bacterial leaflet. Most have shown broad spectrum activity, adequate potency, and minimal resistance. Considering these peptides have been active against pathogens for millions of years and have not developed any broad resistance, they are of particular interest to study. We have characterized the 3D structure, activity, and behavior of NA-CATH, a 34 amino acid CAMP from the Naja Atra snake. NMR studies reveal a single straight amphipathic α-helix with a disordered tail. Using one and two phase liposomes, we have found that lipid composition and the presence of phase separation affect the activity and behavior of NA-CATH. Fluorescence leakage and requenching assays indicate that the presence of phase separation increases leakage activity and the anionic lipid locale affects the leakage mechanism.
- Published
- 2015
36. Mitochondrial and microsomal ferric b5 cytochromes exhibit divergent conformational plasticity in the context of a common fold
- Author
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An Wang, Mario Simeonov, Mario Rivera, Michael A. Massiah, Adriana Altuve, Margaret A. Eastman, and David R. Benson
- Subjects
Models, Molecular ,Protein Folding ,Stereochemistry ,Molecular Sequence Data ,Mitochondria, Liver ,Plasticity ,Biochemistry ,Protein Structure, Secondary ,chemistry.chemical_compound ,medicine ,Side chain ,Animals ,Amino Acid Sequence ,Sequence Homology, Amino Acid ,Cytochrome b ,Chemistry ,Nuclear magnetic resonance spectroscopy ,OM cytochrome b ,Rats ,Cytochromes b5 ,Microsome ,Microsomes, Liver ,Ferric ,Thermodynamics ,medicine.drug ,Hemin - Abstract
Native-state hydrogen-deuterium exchange (HDX) monitored by NMR spectroscopy has been used to compare conformational plasticity in ferric rat liver outer mitochondrial membrane cytochrome b 5 (rOM b 5 ) and ferric bovine liver microsomal cytochrome b 5 (bMc b 5 ). Analysis of the data indicated that rOM b 5 is the less conformationally flexible protein on the time scale probed by the HDX experiments. The data also suggest a likely contributor to the much higher kinetic barrier for the release of hemin from OM b 5 s in comparison to Mc b 5 s, a characteristic that may be to a large extent the source of their divergent functional properties. Specifically, the data indicate that conformational mobility within helices a4 and a5, which flank the loop harboring axial ligand His63, is considerably more restricted in rOM b 5 than in bMc b 5 . The lower conformational flexibility of a4 and α5 in rOM b 5 can reasonably be attributed to more extensive hydrophobic packing in that region of the protein, arising from two conserved side chain packing motifs in OM cytochrome b 5 s [Altuve, A., Wang, L., Benson, D. R., and Rivera, M. (2004) Biochem. Biophys. Res. Commun. 314, 602-609].
- Published
- 2005
37. Structures and mechanisms of Nudix hydrolases
- Author
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Sandra B. Gabelli, Lin-Woo Kang, Zuyong Xia, L.M. Amzel, Patricia M. Legler, Hugo F. Azurmendi, Michael A. Massiah, V. Saraswat, Albert S. Mildvan, and Mario A. Bianchet
- Subjects
Models, Molecular ,Stereochemistry ,Cations, Divalent ,Amino Acid Motifs ,Biophysics ,Glycine ,Glutamic Acid ,Arginine ,Ligands ,Biochemistry ,Nudix hydrolase ,Catalysis ,Protein Structure, Secondary ,Divalent ,Substrate Specificity ,Nucleophile ,Hydrolase ,Nucleophilic substitution ,Organic chemistry ,Amino Acid Sequence ,Pyrophosphatases ,Molecular Biology ,Nuclear Magnetic Resonance, Biomolecular ,Histidine ,chemistry.chemical_classification ,Molecular Structure ,Chemistry ,Hydrolysis ,Lysine ,Leaving group ,Electron Spin Resonance Spectroscopy ,Water ,Hydrogen Bonding ,Lewis acid catalysis ,Models, Structural ,Kinetics ,Dinucleoside Phosphates - Abstract
Nudix hydrolases catalyze the hydrolysis of n ucleoside d iphosphates linked to other moieties, X , and contain the sequence motif or Nudix box, GX 5 EX 7 REUXEEXGU. The mechanisms of Nudix hydrolases are highly diverse in the position on the substrate at which nucleophilic substitution occurs, and in the number of required divalent cations. While most proceed by associative nucleophilic substitutions by water at specific internal phosphorus atoms of a diphosphate or polyphosphate chain, members of the GDP-mannose hydrolase sub-family catalyze dissociative nucleophilic substitutions, by water, at carbon. The site of substitution is likely determined by the positions of the general base and the entering water. The rate accelerations or catalytic powers of Nudix hydrolases range from 10 9 - to 10 12 -fold. The reactions are accelerated 10 3 –10 5 -fold by general base catalysis by a glutamate residue within, or beyond the Nudix box, or by a histidine beyond the Nudix box. Lewis acid catalysis, which contributes ⩾10 3 –10 5 -fold to the rate acceleration, is provided by one, two, or three divalent cations. One divalent cation is coordinated by two or three conserved residues of the Nudix box, the initial glycine and one or two glutamate residues, together with a remote glutamate or glutamine ligand from beyond the Nudix box. Some Nudix enzymes require one (MutT) or two additional divalent cations (Ap 4 AP), to neutralize the charge of the polyphosphate chain, to help orient the attacking hydroxide or oxide nucleophile, and/or to facilitate the departure of the anionic leaving group. Additional catalysis (10–10 3 -fold) is provided by the cationic side chains of lysine and arginine residues and by H-bond donation by tyrosine residues, to orient the general base, or to promote the departure of the leaving group. The overall rate accelerations can be explained by both independent and cooperative effects of these catalytic components.
- Published
- 2004
38. XLOS-Observed Mutations of MID1 Bbox1 Domain Cause Domain Unfolding
- Author
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Michael A. Massiah, Omotolani Babatunde, Katharine M. Wright, Haijuan Du, and Kuanlin Wu
- Subjects
Male ,Models, Molecular ,EGF-like domain ,Ubiquitin-Protein Ligases ,Science ,Protein domain ,Biophysics ,Biology ,Biochemistry ,Protein Chemistry ,HAMP domain ,Esophagus ,Protein structure ,EVH1 domain ,Mutant protein ,Humans ,Amino Acid Sequence ,Protein Phosphatase 2 ,Hypospadias ,Multidisciplinary ,Hypertelorism ,Ubiquitination ,Biology and Life Sciences ,Proteins ,Nuclear Proteins ,Genetic Diseases, X-Linked ,Protein tertiary structure ,Protein Structure, Tertiary ,Cleft Palate ,Zinc ,Mutation ,Microtubule Proteins ,Medicine ,Research Article ,Transcription Factors ,Binding domain - Abstract
MID1 catalyzes the ubiquitination of the protein alpha4 and the catalytic subunit of protein phosphatase 2A. Mutations within the MID1 Bbox1 domain are associated with X-linked Opitz G syndrome (XLOS). Our functional assays have shown that mutations of Ala130 to Val or Thr, Cys142 to Ser and Cys145 to Thr completely disrupt the polyubiquitination of alpha4. Using NMR spectroscopy, we characterize the effect of these mutations on the tertiary structure of the Bbox1 domain by itself and in tandem with the Bbox2 domain. The mutation of either Cys142 or Cys145, each of which is involved in coordinating one of the two zinc ions, results in the collapse of signal dispersion in the HSQC spectrum of the Bbox1 domain indicating that the mutant protein structure is unfolded. Each mutation caused the coordination of both zinc ions, which are ∼ 13 Å apart, to be lost. Although Ala130 is not involved in the coordination of a zinc ion, the Ala130Thr mutant Bbox1 domain yields a poorly dispersed HSQC spectrum similar to those of the Cys142Ser and Cys145Thr mutants. Interestingly, neither cysteine mutation affects the structure of the adjacent Bbox2 domain when the two Bbox domains are engineered in their native tandem Bbox1-Bbox2 protein construct. Dynamic light scattering measurements suggest that the mutant Bbox1 domain has an increased propensity to form aggregates compared to the wild type Bbox1 domain. These studies provide insight into the mechanism by which mutations observed in XLOS affect the structure and function of the MID1 Bbox1 domain.
- Published
- 2014
39. Mechanistic implications of methylglyoxal synthase complexed with phosphoglycolohydroxamic acid as observed by X-ray crystallography and NMR spectroscopy
- Author
-
Michael A. Massiah, Gregory T. Marks, Albert S. Mildvan, David H. T. Harrison, and Thomas K. Harris
- Subjects
Stereochemistry ,Macromolecular Substances ,Carbon-Oxygen Lyases ,Methylglyoxal synthase ,Chemical Fractionation ,Crystallography, X-Ray ,Hydroxamic Acids ,Biochemistry ,Binding, Competitive ,Triosephosphate isomerase ,chemistry.chemical_compound ,DHAP ,Escherichia coli ,Enzyme Inhibitors ,Nuclear Magnetic Resonance, Biomolecular ,Dihydroxyacetone phosphate ,Aspartic Acid ,Binding Sites ,biology ,Methylglyoxal ,Nuclear magnetic resonance spectroscopy ,Lyase ,Enol ,Recombinant Proteins ,Glycolates ,Crystallography ,Kinetics ,chemistry ,Amino Acid Substitution ,biology.protein ,Asparagine ,Protons ,Triose-Phosphate Isomerase - Abstract
Methylglyoxal synthase (MGS) and triosephosphate isomerase (TIM) share neither sequence nor structural similarities, yet the reactions catalyzed by both enzymes are similar, in that both initially convert dihydroxyacetone phosphate to a cis-enediolic intermediate. This enediolic intermediate is formed from the abstraction of the pro-S C3 proton of DHAP by Asp-71 of MGS or the pro-R C3 proton of DHAP by Glu-165 of TIM. MGS then catalyzes the elimination of phosphate from this enediolic intermediate to form the enol of methylglyoxal, while TIM catalyzes proton donation to C2 to form D-glyceraldehyde phosphate. A competitive inhibitor of TIM, phosphoglycolohydroxamic acid (PGH) is found to be a tight binding competitive inhibitor of MGS with a K(i) of 39 nM. PGH's high affinity for MGS may be due in part to a short, strong hydrogen bond (SSHB) from the NOH of PGH to the carboxylate of Asp-71. Evidence for this SSHB is found in X-ray, 1H NMR, and fractionation factor data. The X-ray structure of the MGS homohexamer complexed with PGH at 2.0 A resolution shows this distance to be 2.30-2.37 +/- 0.24 A. 1H NMR shows a PGH-dependent 18.1 ppm signal that is consistent with a hydrogen bond length of 2.49 +/- 0.02 A. The D/H fractionation factor (phi = 0.43 +/- 0.02) is consistent with a hydrogen bond length of 2.53 +/- 0.01 A. Further, 15N NMR suggests a significant partial positive charge on the nitrogen atom of bound PGH, which could strengthen hydrogen bond donation to Asp-71. Both His-98 and His-19 are uncharged in the MGS-PGH complex on the basis of the chemical shifts of their Cdelta and C(epsilon) protons. The crystal structure reveals that Asp-71, on the re face of PGH, and His-19, on the si face of PGH, both approach the NO group of the analogue, while His-98, in the plane of PGH, approaches the carbonyl oxygen of the analogue. The phosphate group of PGH accepts nine hydrogen bonds from seven residues and is tilted out of the imidate plane of PGH toward the re face. Asp-71 and phosphate are thus positioned to function as the base and leaving group, respectively, in a concerted suprafacial 1,4-elimination of phosphate from the enediolic intermediate in the second step of the MGS reaction. Combined, these data suggest that Asp-71 is the one base that initially abstracts the C3 pro-S proton from DHAP and subsequently the 3-OH proton from the enediolic intermediate. This mechanism is compared to an alternative TIM-like mechanism for MGS, and the relative merits of both mechanisms are discussed.
- Published
- 2001
40. Short, strong hydrogen bonds at the active site of human acetylcholinesterase: proton NMR studies
- Author
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Joseph L. Johnson, Putta Mallikarjuna Reddy, Michael A. Massiah, Albert S. Mildvan, Carol Viragh, Ildiko M. Kovach, and Terrone L. Rosenberry
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Stereochemistry ,Organophosphonates ,Torpedo ,Biochemistry ,Paraoxon ,Catalysis ,Adduct ,Nitrophenols ,chemistry.chemical_compound ,Catalytic Domain ,Catalytic triad ,Imidazole ,Animals ,Humans ,Nuclear Magnetic Resonance, Biomolecular ,Histidine ,Binding Sites ,biology ,Chemistry ,Hydrogen bond ,Active site ,Acetophenones ,Hydrogen Bonding ,Hydrogen-Ion Concentration ,Recombinant Proteins ,Proton NMR ,biology.protein ,Acetylcholinesterase ,Cholinesterase Inhibitors ,Protons ,Dimerization - Abstract
Cholinesterases use a Glu-His-Ser catalytic triad to enhance the nucleophilicity of the catalytic serine. We have previously shown by proton NMR that horse serum butyryl cholinesterase, like serine proteases, forms a short, strong hydrogen bond (SSHB) between the Glu-His pair upon binding mechanism-based inhibitors, which form tetrahedral adducts, analogous to the tetrahedral intermediates in catalysis [Viragh, C., et al. (2000) Biochemistry 39, 16200-16205]. We now extend these studies to human acetylcholinesterase, a 136 kDa homodimer. The free enzyme at pH 7.5 shows a proton resonance at 14.4 ppm assigned to an imidazole NH of the active-site histidine, but no deshielded proton resonances between 15 and 21 ppm. Addition of a 3-fold excess of the mechanism-based inhibitor m-(N,N,N-trimethylammonio)trifluoroacetophenone (TMTFA) induced the complete loss of the 14.4 ppm signal and the appearance of a broad, deshielded resonance of equal intensity with a chemical shift delta of 17.8 ppm and a D/H fractionation factor phi of 0.76 +/- 0.10, consistent with a SSHB between Glu and His of the catalytic triad. From an empirical correlation of delta with hydrogen bond lengths in small crystalline compounds, the length of this SSHB is 2.62 +/- 0.02 A, in agreement with the length of 2.63 +/- 0.03 A, independently obtained from phi. Upon addition of a 3-fold excess of the mechanism-based inhibitor 4-nitrophenyl diethyl phosphate (paraoxon) to the free enzyme at pH 7.5, and subsequent deethylation, two deshielded resonances of unequal intensity appeared at 16.6 and 15.5 ppm, consistent with SSHBs with lengths of 2.63 +/- 0.02 and 2.65 +/- 0.02 A, respectively, suggesting conformational heterogeneity of the active-site histidine as a hydrogen bond donor to either Glu-327 of the catalytic triad or to Glu-199, also in the active site. Conformational heterogeneity was confirmed with the methylphosphonate ester anion adduct of the active-site serine, which showed two deshielded resonances of equal intensity at 16.5 and 15.8 ppm with phi values of 0.47 +/- 0.10 and 0.49 +/- 0.10 corresponding to average hydrogen bond lengths of 2.59 +/- 0.04 and 2.61 +/- 0.04 A, respectively. Similarly, lowering the pH of the free enzyme to 5.1 to protonate the active-site histidine (pK(a) = 6.0 +/- 0.4) resulted in the appearance of two deshielded resonances, at 17.7 and 16.4 ppm, consistent with SSHBs with lengths of 2.62 +/- 0.02 and 2.63 +/- 0.02 A, respectively. The NMR-derived distances agree with those found in the X-ray structures of the homologous acetylcholinesterase from Torpedo californica complexed with TMTFA (2.66 +/- 0.28 A) and sarin (2.53 +/- 0.26 A) and at low pH (2.52 +/- 0.25 A). However, the order of magnitude greater precision of the NMR-derived distances establishes the presence of SSHBs at the active site of acetylcholinesterase, and detect conformational heterogeneity of the active-site histidine. We suggest that the high catalytic power of cholinesterases results in part from the formation of a SSHB between Glu and His of the catalytic triad.
- Published
- 2001
41. The structural basis for the perturbed pKa of the catalytic base in 4-oxalocrotonate tautomerase: kinetic and structural effects of mutations of Phe-50
- Author
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Thomas K. Harris, Christian P. Whitman, Michael A. Massiah, Albert S. Mildvan, and Robert M. Czerwinski
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Models, Molecular ,Proline ,Stereochemistry ,Phenylalanine ,Mutant ,Molecular Sequence Data ,Biochemistry ,Polymerase Chain Reaction ,Catalysis ,Structure-Activity Relationship ,Computational chemistry ,Escherichia coli ,Amino Acid Sequence ,Isomerases ,Nuclear Magnetic Resonance, Biomolecular ,Alanine ,biology ,Nitrogen Isotopes ,Chemistry ,Circular Dichroism ,Wild type ,Titrimetry ,Active site ,Nuclear magnetic resonance spectroscopy ,Hydrogen-Ion Concentration ,Recombinant Proteins ,Kinetics ,Models, Chemical ,biology.protein ,4-Oxalocrotonate tautomerase ,Proton NMR ,Mutagenesis, Site-Directed ,Tyrosine ,Two-dimensional nuclear magnetic resonance spectroscopy ,Heteronuclear single quantum coherence spectroscopy - Abstract
The amino-terminal proline of 4-oxalocrotonate tautomerase (4-OT) functions as the general base catalyst in the enzyme-catalyzed isomerization of beta,gamma-unsaturated enones to their alpha,beta-isomers because of its unusually low pK(a) of 6.4 +/- 0.2, which is 3 units lower than that of the model compound, proline amide. Recent studies show that this abnormally low pK(a) is not due to the electrostatic effects of nearby cationic residues (Arg-11, Arg-39, and Arg-61) [Czerwinski, R. M., Harris, T. K., Johnson, Jr., W. H., Legler, P. M., Stivers, J. T., Mildvan, A. S., and Whitman, C. P. (1999) Biochemistry 38, 12358-12366]. Hence, it may result solely from a low local dielectric constant of 14.7 +/- 0.8 at the otherwise hydrophobic active site. Support for this mechanism comes from the study of mutants of the active site Phe-50, which is 5.8 A from Pro-1 and is one of 12 apolar residues within 9 A of Pro-1. Replacing Phe-50 with Tyr does not significantly alter k(cat) or K(m) and results in a pK(a) of 6.0 +/- 0.1 for Pro-1 as determined by (15)N NMR spectroscopy, comparable to that observed for wild type. (1)H-(15)N HSQC and 3D (1)H-(15)N NOESY HSQC spectra of the F50Y mutant demonstrate its conformation to be very similar to that of the wild-type enzyme. In the F50Y mutant, the pK(a) of Tyr-50 is increased by two units from that of a model compound N-acetyl-tyrosine amide to 12.2 +/- 0.3, as determined by UV and (1)H NMR titrations, yielding a local dielectric constant of 13.4 +/- 1.7, in agreement with the value of 13.7 +/- 0.3 determined from the decreased pK(a) of Pro-1 in this mutant. In the F50A mutant, the pK(a) of Pro-1 is 7.3 +/- 0.1 by (15)N NMR titration, comparable to the pK(a) of 7.6 +/- 0.2 found in the pH vs k(cat)/K(m) rate profile, and is one unit greater than that of the wild-type enzyme, indicating an increase in the local dielectric constant to a value of 21.2 +/- 2.6. A loss of structure of the beta-hairpin from residues 50 to 57, which covers the active site, and is the site of the mutation, is indicated by the disappearance in the F50A mutant of four interstrand NOEs and one turn NOE found in wild-type 4-OT. (1)H-(15)N HSQC spectra of the F50A mutant reveal widespread and large changes in the backbone (15)N and NH chemical shifts including those of Gly residues 48, 51, 53, and 54 causing their loss of dispersion at 23 degrees C and their disappearance at 43 degrees C due to rapid exchange with solvent. These observations confirm that the active site of the F50A mutant is more accessible to the external aqueous environment, causing an increase in the local dielectric constant and in the pK(a) of Pro-1. In addition, the F50A mutation decreased k(cat) 167-fold and increased K(m) 11-fold from those of the wild-type enzyme, suggesting an important role for the hydrophobic environment in catalysis, beyond that of decreasing the pK(a) of Pro-1. The F50I and F50V mutations destabilize the protein and decrease k(cat) by factors of 58 and 1.6, and increase K(m) by 3.3- and 3.8-fold, respectively.
- Published
- 2001
42. Solution structure of Delta5-3-ketosteroid isomerase complexed with the steroid 19-nortestosterone hemisuccinate
- Author
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Michael A. Massiah, Albert S. Mildvan, and Apostolos G. Gittis, and Chitrananda Abeygunawardana
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Turn (biochemistry) ,Crystallography ,chemistry.chemical_compound ,Heteronuclear molecule ,Stereochemistry ,Chemistry ,Hydrogen bond ,Dimer ,Ketosteroid ,Isomerase ,Dihedral angle ,Biochemistry ,Protein secondary structure - Abstract
The solution structure of the ketosteroid isomerase homodimer complexed with the product analogue 19-nortestosterone hemisuccinate (19-NTHS) was solved by heteronuclear multidimensional NMR methods using 1647 distance restraints, 77 dihedral angle (φ) restraints, and 67 hydrogen bond restraints per monomer. The refined secondary structure of each subunit consists of three α-helices, eight β-strands, four turns, and two β-bulges. The β-strands form a mixed β-sheet. One of the five proline residues, Pro-39, is cis and begins a nonclassical turn. A self-consistent ensemble of 15 tertiary/quaternary structures of the enzyme dimer−steroid complex, with no distance violations greater than 0.35 A, was generated by simulated annealing and energy minimization with the program X-PLOR. The mean pairwise RMSD of the secondary structural elements was 0.63 A for the average subunit and 1.25 A for the dimer. Within each subunit, the three α-helices are packed onto the concave surface of the β-sheet with a groove between...
- Published
- 1999
43. Comparison of the NMR and X-ray structures of the HIV-1 matrix protein: evidence for conformational changes during viral assembly
- Author
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Wesley I. Sundquist, Michael F. Summers, Christopher P. Hill, Michael A. Massiah, David K. Worthylake, and Allyson M. Christensen
- Subjects
Conformational change ,Viral matrix protein ,Magnetic Resonance Spectroscopy ,Chemistry ,HIV Antigens ,Protein Conformation ,Virus Assembly ,Gene Products, gag ,Trimer ,Nuclear Overhauser effect ,Nuclear magnetic resonance spectroscopy ,Viral membrane ,Crystallography, X-Ray ,Biochemistry ,gag Gene Products, Human Immunodeficiency Virus ,Crystallography ,Viral Proteins ,Virion assembly ,Helix ,Humans ,Molecular Biology ,Research Article - Abstract
The three-dimensional solution- and solid-state structures of the human immunodeficiency virus type-1 (HIV-1) matrix protein have been determined recently in our laboratories by NMR and X-ray crystallographic methods (Massiah et al. 1994. J Mol Biol 244:198-223; Hill et al. 1996. Proc Natl Acad Sci USA 93:3099-3104). The matrix protein exists as a monomer in solution at low millimolar protein concentrations, but forms trimers in three different crystal lattices. Although the NMR and X-ray structures are similar, detailed comparisons have revealed an approximately 6 A displacement of a short 3(10) helix (Pro 66-Gly 71) located at the trimer interface. High quality electron density and nuclear Overhauser effect (NOE) data support the integrity of the X-ray and NMR models, respectively. Because matrix apparently associates with the viral membrane as a trimer, displacement of the 3(10) helix may reflect a physiologically relevant conformational change that occurs during virion assembly and disassembly. These findings further suggest that Pro 66 and Gly 71, which bracket the 3(10) helix, serve as "hinges" that allow the 3(10) helix to undergo this structural reorientation.
- Published
- 1996
44. Three-dimensional structure of the human immunodeficiency virus type 1 matrix protein
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Wesley I. Sundquist, Michael F. Summers, Chiana Paschall, Michael A. Massiah, Mary R. Starich, and Allyson M. Christensen
- Subjects
Models, Molecular ,Magnetic Resonance Spectroscopy ,HIV Antigens ,Protein Conformation ,Molecular Sequence Data ,Gene Products, gag ,gag Gene Products, Human Immunodeficiency Virus ,Protein Structure, Secondary ,Structure-Activity Relationship ,Viral Proteins ,Protein structure ,Structural Biology ,Inner membrane ,Amino Acid Sequence ,Molecular Biology ,Viral matrix protein ,Retroviral matrix protein ,Chemistry ,Cell Membrane ,Hydrogen Bonding ,Nuclear magnetic resonance spectroscopy ,Transmembrane protein ,Protein tertiary structure ,Protein Structure, Tertiary ,Crystallography ,Helix - Abstract
The HIV-1 matrix protein forms an icosahedral shell associated with the inner membrane of the mature virus. Genetic analyses have indicated that the protein performs important functions throughout the viral life-cycle, including anchoring the transmembrane envelope protein on the surface of the virus, assisting in viral penetration, transporting the proviral integration complex across the nuclear envelope, and localizing the assembling virion to the cell membrane. We now report the three-dimensional structure of recombinant HIV-1 matrix protein, determined at high resolution by nuclear magnetic resonance (NMR) methods. The HIV-1 matrix protein is the first retroviral matrix protein to be characterized structurally and only the fourth HIV-1 protein of known structure. NMR signal assignments required recently developed triple-resonance (1H, 13C, 15N) NMR methodologies because signals for 91% of 132 assigned H alpha protons and 74% of the 129 assignable backbone amide protons resonate within chemical shift ranges of 0.8 p.p.m. and 1 p.p.m., respectively. A total of 636 nuclear Overhauser effect-derived distance restraints were employed for distance geometry-based structure calculations, affording an average of 13.0 NMR-derived distance restraints per residue for the experimentally constrained amino acids. An ensemble of 25 refined distance geometry structures with penalties (sum of the squares of the distance violations) of 0.32 A2 or less and individual distance violations under 0.06 A was generated; best-fit superposition of ordered backbone heavy atoms relative to mean atom positions afforded root-mean-square deviations of 0.50 (+/- 0.08) A. The folded HIV-1 matrix protein structure is composed of five alpha-helices, a short 3(10) helical stretch, and a three-strand mixed beta-sheet. Helices I to III and the 3(10) helix pack about a central helix (IV) to form a compact globular domain that is capped by the beta-sheet. The C-terminal helix (helix V) projects away from the beta-sheet to expose carboxyl-terminal residues essential for early steps in the HIV-1 infectious cycle. Basic residues implicated in membrane binding and nuclear localization functions cluster about an extruded cationic loop that connects beta-strands 1 and 2. The structure suggests that both membrane binding and nuclear localization may be mediated by complex tertiary structures rather than simple linear determinants.
- Published
- 1994
45. XLOS-observed mutations of MID1 Bbox1 domain cause domain unfolding.
- Author
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Katharine M Wright, Kuanlin Wu, Omotolani Babatunde, Haijuan Du, and Michael A Massiah
- Subjects
Medicine ,Science - Abstract
MID1 catalyzes the ubiquitination of the protein alpha4 and the catalytic subunit of protein phosphatase 2A. Mutations within the MID1 Bbox1 domain are associated with X-linked Opitz G syndrome (XLOS). Our functional assays have shown that mutations of Ala130 to Val or Thr, Cys142 to Ser and Cys145 to Thr completely disrupt the polyubiquitination of alpha4. Using NMR spectroscopy, we characterize the effect of these mutations on the tertiary structure of the Bbox1 domain by itself and in tandem with the Bbox2 domain. The mutation of either Cys142 or Cys145, each of which is involved in coordinating one of the two zinc ions, results in the collapse of signal dispersion in the HSQC spectrum of the Bbox1 domain indicating that the mutant protein structure is unfolded. Each mutation caused the coordination of both zinc ions, which are ∼ 13 Å apart, to be lost. Although Ala130 is not involved in the coordination of a zinc ion, the Ala130Thr mutant Bbox1 domain yields a poorly dispersed HSQC spectrum similar to those of the Cys142Ser and Cys145Thr mutants. Interestingly, neither cysteine mutation affects the structure of the adjacent Bbox2 domain when the two Bbox domains are engineered in their native tandem Bbox1-Bbox2 protein construct. Dynamic light scattering measurements suggest that the mutant Bbox1 domain has an increased propensity to form aggregates compared to the wild type Bbox1 domain. These studies provide insight into the mechanism by which mutations observed in XLOS affect the structure and function of the MID1 Bbox1 domain.
- Published
- 2014
- Full Text
- View/download PDF
46. MID1 catalyzes the ubiquitination of protein phosphatase 2A and mutations within its Bbox1 domain disrupt polyubiquitination of alpha4 but not of PP2Ac.
- Author
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Haijuan Du, Kuanlin Wu, Alma Didoronkute, Marcus V A Levy, Nimish Todi, Anna Shchelokova, and Michael A Massiah
- Subjects
Medicine ,Science - Abstract
MID1 is a microtubule-associated protein that belongs to the TRIM family. MID1 functions as an ubiquitin E3 ligase, and recently was shown to catalyze the polyubiquitination of, alpha4, a protein regulator of protein phosphatase 2A (PP2A). It has been hypothesized that MID1 regulates PP2A, requiring the intermediary interaction with alpha4. Here we report that MID1 catalyzes the in vitro ubiquitination of the catalytic subunit of PP2A (PP2Ac) in the absence of alpha4. In the presence of alpha4, the level of PP2Ac ubiquitination is reduced. Using the MID1 RING-Bbox1-Bbox2 (RB1B2) construct containing the E3 ligase domains, we investigate the functional effects of mutations within the Bbox domains that are identified in patients with X-linked Opitz G syndrome (XLOS). The RB1B2 proteins harboring the C142S, C145T, A130V/T mutations within the Bbox1 domain and C195F mutation within the Bbox2 domain maintain auto-polyubiquitination activity. Qualitatively, the RB1B2 proteins containing these mutations are able to catalyze the ubiquitination of PP2Ac. In contrast, the RB1B2 proteins with mutations within the Bbox1 domain are unable to catalyze the polyubiquitination of alpha4. These results suggest that unregulated alpha4 may be the direct consequence of these natural mutations in the Bbox1 domain of MID1, and hence alpha4 could play a greater role to account for the increased amount of PP2A observed in XLOS-derived fibroblasts.
- Published
- 2014
- Full Text
- View/download PDF
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