45 results on '"Inouye, Masayori"'
Search Results
2. Signaling by Transmembrane Proteins Shifts Gears
- Author
-
Inouye, Masayori
- Subjects
Membrane proteins ,Nuclear magnetic resonance ,Biological sciences - Abstract
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.cell.2006.08.024 Byline: Masayori Inouye (1) Abstract: The HAMP domain is present in a large number of transmembrane proteins in prokaryotes including histidine kinases, adenylyl cyclases, chemotaxis receptors, and phosphatases. In this issue of Cell, report the NMR structure of a HAMP domain and present data suggesting that it transduces signals through a simple rotation of its four-helix parallel coiled coil. Author Affiliation: (1) Department of Biochemistry, Robert Wood Johnson Medical School, 675 Hoes Lane, Piscataway, NJ 08854, USA
- Published
- 2006
3. Bacillus subtilis MazF-bs (EndoA) is a UACAU-specific mRNA interferase
- Author
-
Park, Jung-Ho, Yamaguchi, Yoshihiro, and Inouye, Masayori
- Published
- 2011
- Full Text
- View/download PDF
4. His-Asp phosphorelay: two components or more?
- Author
-
Inouye, Masayori
- Subjects
Cellular signal transduction -- Bibliography ,Biological sciences - Abstract
The book 'Two-Component Signal Transduction' provides an up-to-date compilation of research done on the signal transduction system in prokaryotes that utilizes the reversible histidine-aspartate phosphorelay system, the so-called 'two-component' system. Researchers are made to note that the signal pathway has been shown to consist of several components in recent researches and that nomenclature in this field of research needs to be systematized. The book is considered an excellent material for researchers in signal transduction.
- Published
- 1996
5. Chapter 12 mRNA Interferases, Sequence‐Specific Endoribonucleases from the Toxin–Antitoxin Systems.
- Author
-
Yamaguchi, Yoshihiro and Inouye, Masayori
- Abstract
Escherichia coli contains a large number of suicide or toxin genes, whose expression leads to cell growth arrest and eventual cell death. One such toxin, MazF, is an ACA‐specific endoribonuclease, termed “mRNA interferase.”E. coli contains other mRNA interferases with different sequence specificities, which are considered to play important roles in growth regulation under stress conditions, and also in eliminating stress‐damaged cells from a population. Recently, MazF homologues with 5‐base recognition sequences have been identified, for example, those from Mycobacterium tuberculosis. These sequences are significantly underrepresented in the genes for protein families playing a role in the immunity and pathogenesis of M. tuberculosis. An mRNA interferase in Myxococcus xanthus is essential for programmed cell death during fruiting body formation. We propose that mRNA interferases play roles not only in cell growth regulation and programmed cell death, but also in regulation of specific gene expression (either positively or negatively) in bacteria. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
6. The Inhibitory Mechanism of Protein Synthesis by YoeB, an Escherichia colI Toxin.
- Author
-
Yonglong Zhang and Inouye, Masayori
- Subjects
- *
PROTEIN synthesis , *ESCHERICHIA coli , *BACTERIAL toxins , *MESSENGER RNA , *RIBOSOMES , *TRANSFER RNA , *BIOCHEMISTRY - Abstract
YoeB is a toxin encoded by the yefM-yoeB antitoxin-toxin operon in the Escherichia coli genome. Here we show that YoeB, a highly potent protein synthesis inhibitor, specifically blocks translation initiation. In in vivo primer extension experiments using two different mRNAs, a major band was detected after YoeB induction at three bases downstream of the initiation codon at 2.5 mm. An identical band was also detected in in vitro toeprinting experiments after the addition of YoeB to the reaction mixtures containing 70 S ribosomes and the same mRNAs, even in the absence of tRNAfMet. Notably, this band was not detected in the presence of YoeB alone, indicating that YoeB by itself does not have endoribonuclease activity under the conditions used. The 70 S ribosomes increased upon YoeB induction, and YoeB was found to be specifically associated with 50 S subunits. Using tetracycline and hygromycin B, we demonstrated that YoeB binds to the 50 S ribosomal subunit in 70 S ribosomes and interacts with the A site leading to mRNA cleavage at this site. As a result, the 3′-end portion of the mRNA was released from ribosomes, and translation initiation was effectively inhibited. These results demonstrate that YoeB primarily inhibits translation initiation. [ABSTRACT FROM AUTHOR]
- Published
- 2009
- Full Text
- View/download PDF
7. The intramolecular chaperone-mediated protein folding
- Author
-
Chen, Yu-Jen and Inouye, Masayori
- Subjects
- *
MOLECULAR chaperones , *PROTEIN folding , *AMINO acid sequence , *PROTEOLYTIC enzymes , *MOLECULAR biology , *BIOCHEMISTRY - Abstract
Some proteins have evolved to contain a specific sequence as an intramolecular chaperone, which is essential for protein folding but not required for protein function, as it is removed after the protein is folded by autoprocessing or by an exogenous protease. To date, a large number of sequences encoded as N-terminal or C-terminal extensions have been identified to function as intramolecular chaperones. An increasing amount of evidence has revealed that these intramolecular chaperones play an important role in protein folding both in vivo and in vitro. Here, we summarize recent studies on intramolecular chaperone-assisted protein folding and discuss the mechanisms as to how intramolecular chaperones play roles in protein folding. [Copyright &y& Elsevier]
- Published
- 2008
- Full Text
- View/download PDF
8. Complex Formation between a Putative 66-Residue Thumb Domain of Bacterial Reverse Transcriptase RT-Ec86 and the Primer Recognition RNA.
- Author
-
Inouye, Masayori, Ke, Haiping, Yashio, Ariko, Yamanaka, Kunitoshi, Nariya, Hirofumi, Shimamoto, Tadashi, and Inouye, Sumiko
- Subjects
- *
RNA , *ESCHERICHIA coli , *DNA polymerases , *REVERSE transcriptase , *MESSENGER RNA , *NUCLEIC acids - Abstract
Reverse transcriptases (RT) are found in a minor population of Escherichia coli and are responsible for the synthesis of multicopy single-stranded DNA. These RTs specifically recognize RNA structures in their individual primer-template RNAs to initiate cDNA synthesis from the 2'-OH group of a specific internal G residue (branching G residue). Here, we purified the 66-residue, C-terminal fragment of RT-Ec86, RT from E. coli, which is responsible for the synthesis of multicopy single-stranded DNAEc86. This fragment, RT-Ec86-(255-320), was found to consist mainly of α-helical structures on the basis of its CD spectrum, which is consistent with the prediction of this region as the thumb domain from the structural alignment of RT-Ec86 with human immunodeficiency virus-1 RT. RT-Ec86-(255-320) was able to bind to a 28-base synthetic RNA consisting of the 5'-end single-stranded RNA containing the branching G residue and the recognition stem-loop structure in the RT-Ec86 primer-template RNA with a Kd value of 5 × 10-8 M. By stepwise shortening of the 5'-end single-stranded region of the RNA, RT-Ec86-(255-320) was found still to be able to form a stable complex with only the stem-loop structure consisting of an 8-bp stem and a 3-base loop. In this stem-loop structure, the UUU loop was essential for the complex formation. RT-Ec73-(251-316) from another E. coli RT could not bind to the 28-base RNA for RT-Ec86 but could bind to its own stem-loop structure having a 3-base AGU loop. These results support the notion that the highly diverse C-terminal regions of bacterial RTs play an important role in recognizing their own specific primer-template RNA structure for the cDNA priming reaction. [ABSTRACT FROM AUTHOR]
- Published
- 2004
- Full Text
- View/download PDF
9. The RAMP Linker in Histidine Kinase Dimeric Receptors Is Critical for Symmetric Transmembrane Signal Transduction.
- Author
-
Yan Zhu and Inouye, Masayori
- Subjects
- *
CELLULAR signal transduction , *BIOENERGETICS , *PHYSIOLOGICAL control systems , *DIMERS , *OLIGOMERS , *GENETIC mutation - Abstract
The HAMP linker, a common structural element between a sensor and a transmitter module in various sensor proteins, plays an essential role in signal transduction. Here, by in vivo complementation experiments with Tar-EnvZ hybrid receptor mutants in which the HAMP linker forms a heterodimer with Tar and EnvZtype subunits, we found that mutations at one linker only affect the function of EnvZ in the same subunit. However, the same mutations affect the EnvZ function of both subunits when only a Tar or EnvZ-type HAMP linker is used. These results suggest that intersubunit interactions in the HAMP linker normally mediate signal transduction through both subunits in a sensor dimer, whereas the signal is asymmetrically transducer through the linker in a heterodimer. This is the first demonstration that two HAMP linkers in a sensor dimer are functionally coupled for normal signal transduction; however, this functional coupling can be reduced when the HAMP linkers lose their symmetric nature. [ABSTRACT FROM AUTHOR]
- Published
- 2004
- Full Text
- View/download PDF
10. Analysis of the Role of the EnvZ Linker Region in Signal Transduction Using a Chimeric Tar/EnvZ Receptor Protein, Tez1.
- Author
-
Yan Zhu and Inouye, Masayori
- Subjects
- *
CELLULAR signal transduction , *PROTEINS - Abstract
Analyzes the role of the EnvZ linker region in signal transduction using a chimeric Tar/EnvZ receptor protein, Tez1. Inability of Tez1 to respond to aspartate, the ligand for Tar; Adjustment of the transmembrane/linker junction in Tez1; Effects of an Ala residue insertion at different sites in the linker.
- Published
- 2003
- Full Text
- View/download PDF
11. GHKL, an emergent ATPase/kinase superfamily.
- Author
-
Dutta, Rinku and Inouye, Masayori
- Subjects
- *
ADENOSINE triphosphatase , *PROTEIN kinases - Abstract
Explores the significance of the ATPase/kinase gyrase, Hsp90, histidine kinase, MutL (GHKL) superfamily in terms of structure, function and evolution. Topological similarity of the ATP-binding domains; Roles of residues from adjacent domains in ATP-binding and catalysis; Description of the novel ATP-binding Bergerat fold; ATP binding and hydrolysis.
- Published
- 2000
- Full Text
- View/download PDF
12. The first demonstration of the existence of reverse transcriptases in bacteria.
- Author
-
Inouye, Masayori
- Subjects
- *
BACTERIA , *BACTERIOPHAGES , *PROKARYOTES , *REVERSE transcriptase , *MYXOCOCCUS xanthus - Abstract
It has been long thought that reverse transcriptases are unique to the eukaryotes. However, through our research on a peculiar single stranded DNA called msDNA in Myxococcus xanthus , it was predicted that its synthesis requires reverse transcriptases. Subsequently, Lim and Maas as well as our group demonstrated the existence of reverse transcriptases for the production of msDNA. In this review, I describe how the discovery of msDNA led to the discovery of reverse transcriptases in bacteria and discuss the evolutionary significance of the discovery of revise transcriptases in bacteria. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
13. The first discovery of RNA interference by RNA restriction enzymes to inhibit protein synthesis.
- Author
-
Inouye, Masayori
- Subjects
- *
RNA interference , *GENE silencing , *ENZYMES , *PROTEIN synthesis , *RNA - Abstract
In this article, I review how an RNA restriction enzyme, a highly sequence-specific endoribonuclease, was for the first time discovered in 2003 and how the concept of RNA interference using RNA restriction enzymes or mRNA interferases has been developed. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
14. The first application of site-directed mutagenesis using oligonucleotides for studying the function of a protein.
- Author
-
Inouye, Masayori
- Subjects
- *
SITE-specific mutagenesis , *OLIGONUCLEOTIDE synthesis , *DNA polymerases , *LIPOPROTEINS , *BACTERIAL genomes , *GENETIC disorder treatment - Published
- 2016
- Full Text
- View/download PDF
15. The first demonstration of RNA interference to inhibit mRNA function.
- Author
-
Inouye, Masayori
- Subjects
- *
RNA interference , *MESSENGER RNA , *ANTISENSE RNA , *BACTERIAL genetics , *ESCHERICHIA coli , *GENETIC research , *PHYSIOLOGY - Abstract
I review how RNA interference was discovered for the first time in 1984 in our laboratory. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
16. The first determination of DNA sequence of a specific gene.
- Author
-
Inouye, Masayori
- Subjects
- *
NUCLEOTIDE sequence , *BACTERIOPHAGES , *RNA , *GENETIC mutation , *BIOCHEMISTRY , *GENETIC techniques - Abstract
How and when the first DNA sequence of a gene was determined? In 1977, F. Sanger came up with an innovative technology to sequence DNA by using chain terminators, and determined the entire DNA sequence of the 5375-base genome of bacteriophage φX 174 ( Sanger et al., 1977 ). While this Sanger's achievement has been recognized as the first DNA sequencing of genes, we had determined DNA sequence of a gene, albeit a partial sequence, 11 years before the Sanger's DNA sequence (Okada et al., 1966). [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
17. The first attempt for the isolation of an intact mRNA for structure determination.
- Author
-
Inouye, Masayori
- Subjects
- *
MESSENGER RNA , *MOLECULAR structure , *NUCLEOTIDE sequence , *BACTERIAL genetics , *ESCHERICHIA coli , *GENETIC research - Abstract
I review the history of the first mRNA which was isolated for the determination of its RNA sequence from Escherichia coli . [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
18. Functional and Structural Characterization of EnvZ, an Osmosensing Histidine Kinase of E. coli.
- Author
-
Yoshida, Takeshi, Phadtare, Sangita, and Inouye, Masayori
- Abstract
An abstract of the article "Functional and Structural Characterization of EnvZ, an Osmosensing Histidine Kinase of E. coli," by Takeshi Yoshida and colleagues is presented.
- Published
- 2007
- Full Text
- View/download PDF
19. The Design and Development of Tar-EnvZ Chimeric Receptors.
- Author
-
Yoshida, Takeshi, Phadtare, Sangita, and Inouye, Masayori
- Abstract
An abstract of the article "The Design and Development of Tar-EnvZ Chimeric Receptors," by Takeshi Yoshida and colleagues is presented.
- Published
- 2007
- Full Text
- View/download PDF
20. DNA sequence of the promoter region of the ompC gene and the amino acid sequence of the signal peptide of pro-OmpC protein in Escherichia coli
- Author
-
Mizuno, Takeshi, Chou, Mei-Yin, and Inouye, Masayori
- Published
- 1983
- Full Text
- View/download PDF
21. Demonstration of dimer formation of the cytoplasmic domain of a transmembrane osmosensor protein, EnvZ, of Escherichia coli using Ni-histidine tag affinity chromatography
- Author
-
Hidaka, Yuji, Park, Heiyoung, and Inouye, Masayori
- Published
- 1997
- Full Text
- View/download PDF
22. Biochemical characterization of Pkn2, a protein Ser/Thr kinase from Myxococcus xanthus, a Gram-negative developmental bacterium
- Author
-
Udo, Hiroshi, Inouye, Masayori, and Inouye, Sumiko
- Published
- 1997
- Full Text
- View/download PDF
23. Defining Requirements for Collagenase Cleavage in Collagen Type III Using a Bacterial Collagen System.
- Author
-
Zhuoxin Yu, Visse, Robert, Inouye, Masayori, Nagase, Hideaki, and Brodsky, Barbara
- Subjects
- *
COLLAGEN , *COLLAGENASES , *MATRIX metalloproteinases , *BACTERIAL proteins , *CHIMERIC proteins - Abstract
Degradation of fibrillar collagens is important in many physiological and pathological events. These collagens are resistant to most proteases due to the tightly packed triple-helical structure, but are readily cleaved at a specific site by collagenases, selected members of the matrix metalloproteinases (MMPs). To investigate the structural requirements for collagenolysis, varying numbers of GXY triplets from human type III collagen around the collagenase cleavage site were inserted between two triple helix domains of the Scl2 bacterial collagen protein. The original bacterial CL domain was not cleaved by MMP-1 (collagenase 1) or MMP-13 (collagenase 3). The minimum type III sequence necessary for cleavage by the two collagenases was 5 GXY triplets, including 4 residues before and 11 residues after the cleavage site (P4-P11′). Cleavage of these chimeric substrates was not achieved by the catalytic domain of MMP-1 or MMP-13, nor by full-length MMP-3. Kinetic analysis of the chimeras indicated that the rate of cleavage by MMP-1 of the chimera containing six triplets (P7-P11′) of collagen III was similar to that of native collagen III. The collagenase-susceptible chimeras were cleaved very slowly by trypsin, a property also seen for native collagen III, supporting a local structural relaxation of the triple helix near the collagenase cleavage site. The recombinant bacterial-human collagen system characterized here is a good model to investigate the specificity and mechanism of action of collagenases. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
- View/download PDF
24. Dissecting a Bacterial Collagen Domain from Streptococcus pyogenes SEQUENCE AND LENGTH-DEPENDENT VARIATIONS IN TRIPLE HELIX STABILITY AND FOLDING.
- Author
-
Zhuoxin Yu, Brodsky, Barbara, and Inouye, Masayori
- Subjects
- *
COLLAGEN , *STREPTOCOCCUS pyogenes , *AMINO acid sequence , *ESCHERICHIA coli , *EUKARYOTIC cells , *GENETIC mutation - Abstract
To better investigate the relationship between sequence, stability, and folding, the Streptococcus pyogenes collagenous domain CL (Gly-Xaa-Yaa)79 was divided to create three recombinant triple helix subdomains A, B, and C of almost equal size with distinctive amino acid features: an A domain high in polar residues, a B domain containing the highest concentration of Pro residues, and a very highly charged C domain. Each segment was expressed as a monomer, a linear dimer, and a linear trimer fused with the trimerization domain (V domain) in Escherichia coli. All recombinant proteins studied formed stable triple helical structures, but the stability varied depending on the amino acid sequence in the A, B, and C segments and increased as the triple helix got longer. V-AAA was found to melt at a much lower temperature (31.0 °C) than V-ABC (V-CL), whereas V-BBB melted at almost the same temperature (~36-37 °C). When heat-denatured, the V domain enhanced refolding for all of the constructs; however, the folding rate was affected by their amino acid sequences and became reduced for longer constructs. The folding rates of all the other constructs were lower than that of the natural V-ABC protein. Amino acid substitution mutations at all Pro residues in the C fragment dramatically decreased stability but increased the folding rate. These results indicate that the thermostability of the bacterial collagen is dominated by the most stable domain in the same manner as found with eukaryotic collagens. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF
25. MqsR, a Crucial Regulator for Quorum Sensing and Bioflim Formation, Is a GCU-specific mRNA Interferase in Escherichia coli.
- Author
-
Yamaguchi, Yoshihiro, Jung-Ho Park, and Inouye, Masayori
- Subjects
- *
GENES , *OPERONS , *ESCHERICHIA coli , *CELL growth , *MESSENGER RNA , *HOMOLOGY (Biology) - Abstract
The mqsR gene has been shown to be positively regulated by the quorum-sensing autoinducer AI-2, which in turn activates a two-component system, the qseB-qseC operon. This operon plays an important role in biofilm formation in Escherichia cvii. However, its cellular function has remained unknown. Here, we found that 1 base downstream of mqsR there is a gene, ygiT, that is co-transcribed with mqsR. Induction of mqsR caused cell growth arrest, whereas ygiT co-induction recovered cell growth. We demonstrate that MqsR (98 amino acid residues), which has no homology to the well characterized mRNA interferase MazF, is a potent inhibitor of protein synthesis that functions by degrading cellular mRNAs. In vivo and in vitro primer extension experiments showed that MqsR is an mRNA interferase specifically cleaving mRNAs at GCU. The mRNA interferase activity of purified MqsR was inhibited by purified YgiT (131 residues). MqsR forms a stable 2:1 complex with YgiT, and the complex likely functions as a repressor for the mqsR-ygiT operon by specifically binding to two different palindromic sequences present in the 5'-untranslated region of this operon. [ABSTRACT FROM AUTHOR]
- Published
- 2009
- Full Text
- View/download PDF
26. Characterization of YafO, an Escherichia coli Toxin.
- Author
-
Zhang, Yonglong, Yamaguchi, Yoshihiro, and Inouye, Masayori
- Subjects
- *
BACTERIAL toxins , *ESCHERICHIA coli , *OPERONS , *IN vivo toxicity testing , *METHIONINE , *MESSENGER RNA , *PROTEIN synthesis , *TRANSFER RNA , *PHYSIOLOGY - Abstract
YafO is a toxin encoded by the yafN-yafO antitoxin-toxin operon in the Escherichia coli genome. Our results show that YafO inhibits protein synthesis but not DNA or RNA synthesis. The in vivo [35S]methionine incorporation was inhibited within 5 mm after YafO induction. In in vivo primer extension experiments with two different mRNAs, the specific cleavage bands appeared 11-13 bases downstream of the initiation codon, AUG, 2.5 mm after the induction of YafO. An identical band was also detected in in vitro toeprinting experiments when YafO was added to the reaction mixture containing 70 S ribosomes and the same mRNAs even in the absence of tRNAfMet. Notably, this band was not detected in the presence of YafO alone, indicating that YafO by itself does not have endoribonuclease activity under the conditions used. The full-length mRNAs almost completely disappeared 30 mm after YafO induction in in vivo primer extension experiments, consistent with Northern blotting analysis. Over 84% of [35S)methionine-tRNAfMet was released from the translation initiation complex at 5.43 μM YafO in vitro. We demonstrated that the 70 S ribosome peak significantly increased upon YafO induction, and when the 70 S ribosomes dissociated into 50 and 30 S subunits, YafO was found to be associated with 50 S subunits. These results demonstrate that YafO is a ribosome-dependent mRNA interferase inhibiting protein synthesis. [ABSTRACT FROM AUTHOR]
- Published
- 2009
- Full Text
- View/download PDF
27. Inhibitory Mechanism of Escherichia coil RelE-RelB Toxin-Antitoxin Module Involves a Helix Displacement Near an mRNA Interferase Active Site.
- Author
-
Guang-Yao Li, Yonglong Zhang, Inouye, Masayori, and Ikura, Mitsuhiko
- Subjects
- *
ESCHERICHIA coli , *CELL death , *MESSENGER RNA , *PEPTIDES , *ANTITOXINS , *ORGANIC compounds - Abstract
In Escherichia coli, RelE toxin participates in growth arrest and cell death by inducing mRNA degradation at the ribosomal A-site under stress conditions. The NMR structures of a mutant of E. coli RelE toxin, RelER81A/R83A, with reduced toxicity and its complex with an inhibitory peptide from RelB antitoxin, RelBC (Lys47-Leu79), have been determined. In the free RelER81A/R83A structure, helix at the C terminus adopts a closed conformation contacting with the β-sheet core and adjacent loops. In the RelER81A/R83A-RelBC complex, helix α3* of RelBC displaces α4 of RelER81A/R83A from the binding site on the β-sheet core. This helix replacement results in neutralization of a conserved positively charged cluster of RelE by acidic residues from α3* of RelB. The released helix α4 becomes unfolded, adopting an open conformation with increased mobility. The displacement of α4 disrupts the geometry of critical residues, including Arg81 and Tyr87, in a putative active site of RelE toxin. Our structures indicate that RelB counteracts the toxic activity of RelE by displacing α4 helix from the catalytically competent position found in the free RelE structure. [ABSTRACT FROM AUTHOR]
- Published
- 2009
- Full Text
- View/download PDF
28. Finding one of a kind: advances in single-protein production
- Author
-
Falzon, Liliana, Suzuki, Motoo, and Inouye, Masayori
- Subjects
- *
PROTEIN synthesis , *CELLS , *MESSENGER RNA , *ESCHERICHIA coli , *BIOMOLECULES - Abstract
An ultimate goal for any protein production system is to express only the protein of interest without producing other cellular proteins. To date, there are only two established methods that will allow the successful expression of only the protein of interest: the cell-free in vitro protein synthesis system and the in vivo single-protein production (SPP) system. Although single-protein production can be achieved in cell-free systems, it is not easy to completely suppress the production of cellular proteins during the production of a protein of interest in a living cell. However, the finding of a unique sequence-specific mRNA interferase in Escherichia coli led to the development of the SPP system by converting living cells into a bioreactor that produces only a single protein of interest without producing any cellular proteins. This technology not only provides a new high expression system for proteins, but also offers a novel avenue for protein structural studies. [Copyright &y& Elsevier]
- Published
- 2006
- Full Text
- View/download PDF
29. Characterization of the Interactions within the mazEF Addiction Module of Escherichia coli.
- Author
-
Junjie Zhang, Yonglong Zhang, and Inouye, Masayori
- Subjects
- *
CELL death , *TOXINS , *ANTITOXINS , *ESCHERICHIA coli - Abstract
In bacteria, programmed cell death is mediated through the unique genetic system called "addiction module," which consists of a pair of genes encoding a stable toxin and an unstable antitoxin. The mazEF system is known as an addiction module located on the Escherichia coli chromosome. MazF is a stable toxin, and Maze is a labile antitoxin interacting with MazF to form a complex. Maze and the MazE-MazF complex can bind to the mazEF promoter region to regulate the mazEF expression. Here we show that the binding of purified (His)[sub 6]MazE to the mazEF promoter DNA was enhanced by MazF. The site-directed mutations at the conserved amino acid residues in Maze N-terminal region (K7A, R8A, S12A, and R16A) disrupted the DNA binding ability of both (His)[sub 6]MazE and the MazE-MazF(His)[sub 6] complex, suggesting that Maze binds to the mazEF promoter DNA through the N-terminal domain. The ratio of Maze to MazF(His)[sub 6] in the MazE-MazF(His)[sub 6] complex is about 1:2. Because both Maze and MazF(His)[sub 6] exist as dimers by themselves, the MazE-MazF(His)[sub 6] complex (76.9 kDa) is predicted to consist of one Maze dimer and two MazF(His)[sub 6] dimers. The interaction between Maze and MazF was also characterized with the yeast two-hybrid system. It was found that the region from residues 38 to 75 of Maze was required for its binding to MazF. Site-directed mutagenesis at this region revealed that Leu[sup 55] and Leu[sup 58] play an important role in the MazE-MazF complex formation but not in Maze binding to the mazEF promoter DNA. The present results demonstrate that Maze is composed of two domains, the N-terminal DNA-binding domain and the Cterminal domain interacting with MazF. [ABSTRACT FROM AUTHOR]
- Published
- 2003
- Full Text
- View/download PDF
30. Thermotoga maritima MazG Protein Has Both Nucleoside Triphosphate Pyrophosphohydrolase and Pyrophosphatase Activities.
- Author
-
Junjie Zhang, Yonglong Zhang, and Inouye, Masayori
- Subjects
- *
PROTEINS , *NUCLEOSIDES , *PHOSPHATASES - Abstract
Reports that Thermotoga maritima MazG protein, the product of the TM0913 gene, has both nucleoside triphosphate pyrophosphohydrolase and pyrophosphatase activities. Characteristics of MazG proteins; Enzymatic functions of Thermotoga MazG proteins.
- Published
- 2003
- Full Text
- View/download PDF
31. Replacement of All Arginine Residues with Canavanine in MazF-bs mRNA Interferase Changes Its Specificity.
- Author
-
Ishida, Yojiro, Park, Jung-Ho, Mao, Lili, Yamaguchi, Yoshihiro, and Inouye, Masayori
- Subjects
- *
ARGININE , *CANAVANINE , *MESSENGER RNA , *BACILLUS subtilis , *ESCHERICHIA coli - Abstract
Replacement of a specific amino acid residue in a protein with nonnatural analogues is highly challenging because of their cellular toxicity. Wedemonstrate for the first time the replacement of all arginine (Arg) residues in a protein with canavanine (Can), a toxic Arg analogue. All Arg residues in the 5-base specific (UACAU) mRNA interferase from Bacillus subtilis (MazFbs(arg)) were replaced with Can by using the single-protein production system in Escherichia coli. The resulting MazF-bs(can) gained a 6-base recognition sequence, UACAUA, for RNA cleavage instead of the 5-base sequence, UACAU, for MazFbs(arg). Mass spectrometry analysis confirmed that all Arg residues were replaced with Can. The present system offers a novel approach to create new functional proteins by replacing a specific amino acid in a protein with its analogues. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
32. Growth and Translation Inhibition through Sequence-specific RNA Binding by Mycobacterium tuberculosis VapC Toxin.
- Author
-
Sharp, Jared D., Cruz, Jonathan W., Raman, Sahadevan, Inouye, Masayori, Husson, Robert N., and Woychik, Nancy A.
- Subjects
- *
RNA-protein interactions , *MYCOBACTERIUM tuberculosis , *MESSENGER RNA , *MICROBIAL virulence , *ANTIBODY-toxin conjugates - Abstract
The Mycobacterium tuberculosis genome harbors an unusually large number of toxin-antitoxin (TA) modules. Curiously, over half of these are VapBC (virulence-associated protein) family members. Nonetheless, the cellular target, precise mode of action, and physiological role of the VapC toxins in this important pathogen remain unclear. To better understand the function of this toxin family, we studied the features and biochemical properties of a prototype M. tuberculosis VapBC TA system, vapBC-mt4 (Rv0596c-Rv0595c). VapC-mt4 expression resulted in growth arrest, a hallmark of all TA toxins, in Escherichia coli, Mycobacterium smegmatis, and M. tuberculosis. Its expression led to translation inhibition accompanied by a gradual decrease in the steady-state levels of several mRNAs. VapC-mt4 exhibited sequence-specific endoribonuclease activity on mRNA templates at ACGC and AC(A/U)GC sequences. However, the cleavage activity of VapC-mt4 was comparatively weak relative to the TA toxin MazF-mt1 (Rv2801c). Unlike other TA toxins, translation inhibition and growth arrest preceded mRNA cleavage, suggesting that the RNA binding property of VapC-mt4, not RNA cleavage, initiates toxicity. In support of this hypothesis, expression of VapC-mt4 led to an increase in the recovery of total RNA with time in contrast to TA toxins that inhibit translation via direct mRNA cleavage. Additionally, VapC-mt4 exhibited stable, sequence-specific RNA binding in an electrophoretic mobility shift assay. Finally, VapC-mt4 inhibited protein synthesis in a cell-free system without cleaving the corresponding mRNA. Therefore, the activity of VapC-mt4 is mechanistically distinct from other TA toxins because it appears to primarily inhibit translation through selective, stable binding to RNA. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
- View/download PDF
33. Noncog nate Mycobacterium tuberculosis Toxin-Antitoxins Can Physically and Functionally Interact.
- Author
-
Ling Zhu, Sharp, Jared D., Kobayashi, Hiroshi, Woychik, Nancy A., and Inouye, Masayori
- Subjects
- *
IMMUNOGLOBULINS , *ANTIDOTES , *ANTITOXINS , *MESSENGER RNA , *GENOMES - Abstract
The Mycobacterium tuberculosis genome harbors a striking number (>40) of toxin-antitoxin systems. Among them are at least seven MazF orthologs, designated MazF-mt1 through MazF-mt7, four of which have been demonstrated to function as mRNA interferases that selectively target mRNA for cleavage at distinct consensus sequences. As is characteristic of all toxin-antitoxin systems, each of the mazF-mt toxin genes is organized in an operon downstream of putative antitoxin genes. However, only one of the seven putative upstream antitoxins (designated MazE-mt1 through MazE-mt7) has significant sequence similarity to Escherichia coli MazE, the cognate antitoxin for E. coli MazF. Interestingly, the M. tuberculosis genome contains two independent operons encoding E. coli MazE orthologs, but they are not paired with mazF-mt-like genes. Instead, the genes encoding these two MazE orthologs are each paired with proteins containing a PIN domain, indicating that they may be members of the very large VapBC toxin-antitoxin family. We tested a spectrum of pair-wise combinations of cognate and noncognate Mtb toxin-antitoxins using in vivo toxicity and rescue experiments along with in vitro interaction experiments. Surprisingly, we uncovered several examples of noncognate toxin-antitoxin association, even among different families (e.g. MazF toxins and VapB antitoxins). These results challenge the "one toxin for one antitoxin" dogma and suggest that M. tuberculosis may enlist a sophisticated toxin-antitoxin network to alter its physiology in response to environmental cues. [ABSTRACT FROM AUTHOR]
- Published
- 2010
- Full Text
- View/download PDF
34. Crystal Structures of Phd-Doc, HigA, and YeeU Establish Multiple Evolutionary Links between Microbial Growth-Regulating Toxin-Antitoxin Systems
- Author
-
Arbing, Mark A., Handelman, Samuel K., Kuzin, Alexandre P., Verdon, Grégory, Wang, Chi, Su, Min, Rothenbacher, Francesca P., Abashidze, Mariam, Liu, Mohan, Hurley, Jennifer M., Xiao, Rong, Acton, Thomas, Inouye, Masayori, Montelione, Gaetano T., Woychik, Nancy A., and Hunt, John F.
- Subjects
- *
BACTERIAL toxins , *BACTERIAL antitoxins , *MICROBIAL growth , *REGULATION of cell growth , *CRYSTALLOGRAPHY , *ESCHERICHIA coli - Abstract
Summary: Bacterial toxin-antitoxin (TA) systems serve a variety of physiological functions including regulation of cell growth and maintenance of foreign genetic elements. Sequence analyses suggest that TA families are linked by complex evolutionary relationships reflecting likely swapping of functional domains between different TA families. Our crystal structures of Phd-Doc from bacteriophage P1, the HigA antitoxin from Escherichia coli CFT073, and YeeU of the YeeUWV systems from E. coli K12 and Shigella flexneri confirm this inference and reveal additional, unanticipated structural relationships. The growth-regulating Doc toxin exhibits structural similarity to secreted virulence factors that are toxic for eukaryotic target cells. The Phd antitoxin possesses the same fold as both the YefM and NE2111 antitoxins that inhibit structurally unrelated toxins. YeeU, which has an antitoxin-like activity that represses toxin expression, is structurally similar to the ribosome-interacting toxins YoeB and RelE. These observations suggest extensive functional exchanges have occurred between TA systems during bacterial evolution. [ABSTRACT FROM AUTHOR]
- Published
- 2010
- Full Text
- View/download PDF
35. A Streptococcus pyogenes derived collagen-like protein as a non-cytotoxic and non-immunogenic cross-linkable biomaterial
- Author
-
Peng, Yong Y., Yoshizumi, Ayumi, Danon, Stephen J., Glattauer, Veronica, Prokopenko, Olga, Mirochnitchenko, Oleg, Yu, Zhuoxin, Inouye, Masayori, Werkmeister, Jerome A., Brodsky, Barbara, and Ramshaw, John A.M.
- Subjects
- *
STREPTOCOCCUS pyogenes , *COLLAGEN , *RECOMBINANT proteins , *ANTINEOPLASTIC agents , *BIOMEDICAL materials , *BODY temperature , *IMMUNOGENETICS , *CELL-mediated cytotoxicity , *PROTEIN crosslinking - Abstract
Abstract: A range of bacteria have been shown to contain collagen-like sequences that form triple-helical structures. Some of these proteins have been shown to form triple-helical motifs that are stable around body temperature without the inclusion of hydroxyproline or other secondary modifications to the protein sequence. This makes these collagen-like proteins particularly suitable for recombinant production as only a single gene product and no additional enzyme needs to be expressed. In the present study, we have examined the cytotoxicity and immunogenicity of the collagen-like domain from Streptococcus pyogenes Scl2 protein. These data show that the purified, recombinant collagen-like protein is not cytotoxic to fibroblasts and does not elicit an immune response in SJL/J and Arc mice. The freeze dried protein can be stabilised by glutaraldehyde cross-linking giving a material that is stable at >37 °C and which supports cell attachment while not causing loss of viability. These data suggest that bacterial collagen-like proteins, which can be modified to include specific functional domains, could be a useful material for medical applications and as a scaffold for tissue engineering. [Copyright &y& Elsevier]
- Published
- 2010
- Full Text
- View/download PDF
36. Mechanism of Stabilization of a Bacterial Collagen Triple Helix in the Absence of Hydroxyproline.
- Author
-
Mohs, Angela, Silva, Teresita, Yoshida, Takeshi, Amin, Ravish, Lukomski, Slawomir, Inouye, Masayori, and Brodsky, Barbara
- Subjects
- *
COLLAGEN , *EXTRACELLULAR matrix proteins , *STREPTOCOCCUS pyogenes , *TRYPSIN , *PHYSICAL biochemistry - Abstract
The Streptococcus pyogenes cell-surface protein Scl2 contains a globular N-terminal domain and a collagen-like domain, (Gly-Xaa-X′aa)79, which forms a triple helix with a thermal stability close to that seen for mammalian collagens. Hyp is a major contributor to triple-helix stability in animal collagens, but is not present in bacteria, which lack prolyl hydroxylase. To explore the basis of bacterial collagen triple-helix stability in the absence of Hyp, biophysical studies were carried out on recombinant Scl2 protein, the isolated collagen-like domain from Scl2, and a set of peptides modeling the Scl2 highly charged repetitive (Gly-Xaa-X′aa)n sequences. At pH 7, CD spectroscopy, dynamic light scattering, and differential scanning calorimetry of the Scl2 protein all showed a very sharp thermal transition near 36 °C, indicating a highly cooperative unfolding of both the globular and triple-helix domains. The collagen-like domain isolated by trypsin digestion showed a sharp transition at the same temperature, with an enthalpy of 12.5 kJ/mol of tripeptide. At low pH, Scl2 and its isolated collagen-like domain showed substantial destabilization from the neutral pH value, with two thermal transitions at 24 and 27 °C, A similar destabilization at low pH was seen for Scl2 charged model peptides, and the degree of destabilization was consistent with the strong pH dependence arising from the GKD tripeptide unit. The Scl2 protein contained twice as much charge as human fibril-forming collagens, and the degree of electrostatic stabilization observed for Scl2 was similar to the contribution Hyp makes to the stability of mammalian collagens. The high enthalpic contribution to the stability of the Scl2 collagenous domain supports the presence of a hydration network in the absence of Hyp. [ABSTRACT FROM AUTHOR]
- Published
- 2007
- Full Text
- View/download PDF
37. Structural and Functional Studies of the HAMP Domain of EnvZ, an Osmosensing Transmembrane Histidine Kinase in Escherichia coli.
- Author
-
Kishii, Ryuta, Faizon, Liliana, Yoshida, Takeshi, Kobayashi, Hiroshi, and Inouye, Masayori
- Subjects
- *
CELLULAR signal transduction , *PROTEIN kinases , *ESCHERICHIA coli , *THERMOPHILIC bacteria , *BIOCHEMISTRY - Abstract
The HAMP domain plays an essential role in signal transduction not only in histidine kinase but also in a number of other signal-transducing receptor proteins. Here we expressed the EnvZ HAMP domain (Arg180-Thr235) with the R218K mutation (termed LRK) or with LRK connected with domain A (Arg180-Arg289) (termed LARK) of EnvZ, an osmosensing transmembrane histidine kinase in Escherichia coli, by fusing it with pro- tein S. The LRK and LARK proteins were purified after removing protein S. The CD analysis of the isolated L protein revealed that it consists of a random structure or is unstructured. This suggests that the EnvZ HAMP domain by itself is unable to form a stable structure and that this structural fragility may be important for its role in signal transduction. Interestingly the substitution of Ala193 in the EnvZ HAMP domain with valine or leucine in TeziAl, a chimeric protein of Tar and EnvZ, caused a constitutive OmpC phenotype. The CD analysis of LARK(A193L) revealed that this mutated HAMP domain possesses considerable secondary structures and that the thermo-stability of this entire LARK(A193L) became substantially lower than that of LARK or just domain A, indicating that the structure of the HAMP domain with the A193L mutation affects the stability of downstream domain A. This results in cooperative thermodenaturation of domain A with the mutated HAMP domain. These results are discussed in light of the recently solved NMR structure of the HAMP domain from a thermophilic bacterium (Hulko, M., Berndt, F., Gruber, M., Linder, J. U., Truffault, V., Schultz, A., Martin, J., Schultz, J. E., Lupas, A. N., and Coles, M. (2006) Cell 126, 929-940). [ABSTRACT FROM AUTHOR]
- Published
- 2007
- Full Text
- View/download PDF
38. Bacterial Bioreactors for High Yield Production of Recombinant Protein.
- Author
-
Suzuki, Motoo, Roy, Rohini, Haiyan Zheng, Woychik, Nancy, and Inouye, Masayori
- Subjects
- *
BACTERIA , *MESSENGER RNA , *PROTEINS , *RECOMBINANT proteins , *CELL-mediated cytotoxicity , *ESCHERICHIA coli , *BIOREACTORS , *GENOMICS - Abstract
We developed a new bacterial expression system that utilizes a combination of attributes (low temperature, induction of an mRNA-specific endoribonuclease causing host cell growth arrest, and culture condensation) to facilitate stable, high level protein expression, almost 30% of total cellular protein, without background protein synthesis. With the use of an optimized vector, exponentially growing cultures could be condensed 40-fold without affecting protein yields, which lowered sample labeling costs to a few percent of the cost of a typical labeling experiment. Because the host cells were completely growth-arrested, toxic amino acids such as selenomethionine and fluorophenylalanine were efficiently incorporated into recombinant proteins in the absence of cytotoxicity. Therefore, this expression system using Escherichia coli as a bioreactor is especially well suited to structural genomics, large-scale protein expressions, and the production of cytotoxic proteins. [ABSTRACT FROM AUTHOR]
- Published
- 2006
- Full Text
- View/download PDF
39. Characterization of mRNA Interferases from Mycobacterium tuberculosis.
- Author
-
Ling Zhu, Yonglong Zhang, Jiah-shin Teh, Junjie Zhang, Connell, Nancy, Rubin, Harvey, and Inouye, Masayori
- Subjects
- *
MESSENGER RNA , *MYCOBACTERIUM tuberculosis , *RNA , *ANTITOXINS , *BACTERIAL genomes , *MICROBIAL genomes - Abstract
mRNA interferases are sequence-specific endoribonucleases encoded by the toxin-antitoxin systems in the bacterial genomes. MazF from Escherichia coli has been shown to be an mRNA interferase that specifically cleaves at ACA sequences in single-stranded RNAs. It has been shown that MazF induction in E. coli effectively inhibits protein synthesis leading to cell growth arrest in the quasi-dormant state. Here we have demonstrated that Mycobacterium tuberculosis contains at least seven genes encoding MazF homologues (MazF-mt1 to -mt7), four of which (MazF-mt1, -mt3, -mt4, and -mt6) caused cell growth arrest when induced in E. coli. MazF-mt1 and MazF-mt6 were purified and characterized for their mRNA interferase specificities. We showed that MazF-mt1 preferentially cleaves the era mRNA between U and A in UAC triplet sequences, whereas MazF-mt6 preferentially cleaves U-rich regions in the era mRNA both in vivo and in vitro. These results indicate that M. tuberculosis contains sequence-specific mRNA interferases, which may play a role in the persistent dormancy of this devastating pathogen in human tissues. [ABSTRACT FROM AUTHOR]
- Published
- 2006
- Full Text
- View/download PDF
40. Transcription Regulation of ompF and ompC by a Single Transcription Factor, OmpR.
- Author
-
Yoshida, Takeshi, Ling Qin, Egger, Linda A., and Inouye, Masayori
- Subjects
- *
ESCHERICHIA coli , *TRANSCRIPTION factors , *GENETIC transcription , *BACTERIAL genetics , *ESCHERICHIA - Abstract
The ompF and ompC genes of Escherichia coli are reciprocally regulated by a single transcription factor, phosphorylated OmpR (OmpR-P), depending upon medium osmolarity. This regulation involves activation of ompF and its repression with concomitant activation of ompC. This occurs through OmpR-P binding to four (F1, F2, F3, and F4) and three (C1, C2, and C3) sites located upstream of the ompF and ompC promoters, respectively, through a novel mechanism, Here we show that there is a distinct OmpR-P binding hierarchy within F1, F2, and F3 sites as well as within C1, C2, and C3 sites. Each of these sites contains two tandem 10-bp OmpR-P-binding subsites, a-site and b-site (from 5′ to 3′ direction). OmpR-P has higher affinity to the downstream b-site than to the upstream a-site in each case. Six OmpR-P molecules bind to F and C sites two-by-two in a discontinuous "galloping" manner. We propose that this tight hierarchical binding of a transcription factor, OmpR, allows distinct stepwise regulation of ompF and ompC transcription, which minimizes their overlapping expression upon changes in the medium osmolarity to achieve the reciprocal expression of ompF and ompC. [ABSTRACT FROM AUTHOR]
- Published
- 2006
- Full Text
- View/download PDF
41. Characterization of ChpBK, an mRNA Interferase from Escherichia coli.
- Author
-
Yonglong Zhang, Ling Zhu, Zhang, Junjie, and Inouye, Masayori
- Subjects
- *
TOXINS , *MESSENGER RNA , *ESCHERICHIA coli , *AMINO acids , *RIBONUCLEASES , *METHIONINE , *BIOCHEMISTRY - Abstract
Escherichia coli contains a number of antitoxin-toxin modules on its chromosome, which are responsible for cell growth arrest and possible cell death. ChpBK is a toxin encoded by the ChpBIK antitoxin-toxin module. This module consists of a pair of genes, chpBI and chpBK encoding antitoxin ChpBI and toxin ChpBK, respectively. ChpBK consists of 116 amino acid residues, and its sequence shows 35% identity and 52% similarity to MazF, another E. coli toxin. MazF has been shown to be a sequence-specific (ACA) endoribonuclease that cleaves cellular mRNAs and effectively blocks protein synthesis and is thus termed as an mRNA interferase. Here we demonstrate that ChpBK is another mRNA interferase in E. coli whose induction effectively blocks cell growth in a manner similar to that of MazF. The protein synthesis as judged by incorporation of [35S]methionine was, however, reduced by only 60% upon ChpBK induction. We demonstrate that ChpBK is a new sequence-specific endoribonuclease that cleaves mRNAs both in vivo and in vitro at the 5′-or 3′-side of the A residue in ACY sequences (Y is U, A, or G). The ChpBK cleavage of a synthetic RNA substrate generated a 2′,3′o cyclic phosphate group at the 3′-end of the 5′-end product and a 5′-OH group at the 5′-end of the 3′-end product in a manner identical to that of MazF. [ABSTRACT FROM AUTHOR]
- Published
- 2005
- Full Text
- View/download PDF
42. Insights into the mRNA Cleavage Mechanism by MazF, an mRNA Interferase.
- Author
-
Yonglong Zhang, Junjie Zhang, Hara, Hiroto, Kato, Ikunoshin, and Inouye, Masayori
- Subjects
- *
MESSENGER RNA , *ESCHERICHIA coli , *TOXINS , *ANTIGENS , *METABOLITES , *PROKARYOTES - Abstract
MazF is an Escherichia coli toxin that is highly conserved among the prokaryotes and plays an important role in growth regulation. When MazF is induced, protein synthesis is effectively inhibited. However, the mechanism of MazF action has been controversial. Here we unequivocally demonstrate that MazF is an endoribonuclease that specifically cleaves mRNAs at ACA sequences. We then demonstrate its enzymatic specificity using short RNA substrates. MazF cleaves RNA at the 5'-end of ACA sequences, yielding a 2',3'-cyclic phosphate at one side and a free 5'-OH group at the other. Using DNA-RNA chimeric substrates containing XACA, the 2'-OH group of residue X was found absolutely essential for MazF cleavage, whereas all the other residues may be deoxyriboses. Therefore, MazF exhibits exquisite site specificity and has utility as an RNA-restriction enzyme for RNA structural studies or as an mRNA interferase to regulate cell growth in prokaryotic and eukaryotic cells. [ABSTRACT FROM AUTHOR]
- Published
- 2005
- Full Text
- View/download PDF
43. Interference of mRNA Function by Sequence-specific Endoribonuclease PemK.
- Author
-
Zhang, Junjie, Zhang, Yonglong, Zhu, Ling, Suzuki, Motoo, and Inouye, Masayori
- Subjects
- *
ESCHERICHIA coli , *CELL death , *TOXINS , *ANTITOXINS , *PLASMIDS , *PROTEIN synthesis , *MESSENGER RNA , *GENOMES - Abstract
In Escherichia coli, programmed cell death is mediated through the system called ’addiction module,’ which consists of a pair of genes encoding a stable toxin and a labile antitoxin. The pemI-pemK system is an addiction module present on plasmid R100. It helps to maintain the plasmid by post-segregational killing in E. coli population. Here we demonstrate that purified PemK, the toxin encoded by the pemI-pemK addiction module, inhibits protein synthesis in an E. coli cell-free system, whereas the addition of PemI, the antitoxin against PemK, resumes the protein synthesis. Further studies reveal that PemK is a sequence-specific endoribonuclease that cleaves mRNAs to inhibit protein synthesis, whereas PemI blocks the endoribonuclease activity of PemK. PemK cleaves only single-stranded RNA preferentially at the 5′ or 3′ side of the A residue in the ’UAH’ sequences (where H is C, A, or U). Upon induction, PemK cleaves cellular mRNAs to effectively block protein synthesis in E. coli. The pemK homologue genes have been identified on the genomes of a wide range of bacteria. We propose that PemK and its homologues form a novel endoribonuclease family that interferes with mRNA function by cleaving cellular mRNAs in a sequence-specific manner. [ABSTRACT FROM AUTHOR]
- Published
- 2004
- Full Text
- View/download PDF
44. Domain Arrangement of Der, a Switch Protein Containing Two GTPase Domains
- Author
-
Robinson, Victoria L., Hwang, Jihwan, Fox, Eileen, Inouye, Masayori, and Stock, Ann M.
- Subjects
- *
GUANOSINE triphosphatase , *MAGNETIC domain , *FERROMAGNETIC materials - Abstract
The EngA subfamily of essential bacterial GTPases has a unique domain structure consisting of two adjacent GTPase domains (GD1 and GD2) and a C-terminal domain. The structure of Thermotoga maritima Der bound to GDP determined at 1.9 A˚ resolution reveals a novel domain arrangement in which the GTPase domains pack at either side of the C-terminal domain. Unexpectedly, the C-terminal domain resembles a KH domain, missing the distinctive RNA recognition elements. Conserved motifs of the nucleotide binding site of GD1 are integral parts of the GD1-KH domain interface, suggesting the interactions between these two domains are directly influenced by the GTP/GDP cycling of the protein. In contrast, the GD2-KH domain interface is distal to the GDP binding site of GD2. [Copyright &y& Elsevier]
- Published
- 2002
- Full Text
- View/download PDF
45. High expression and physical properties of bacterial collagen
- Author
-
Yoshizumi, Ayumi, Yu, Zhuoxin, Thiagarajan, Geetha, Silva, Teresita, Mohs, Angela, Yoshida, Takeshi, Inouye, Masayori, and Brodsky, Barbara
- Published
- 2008
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.