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Interplay of the H-bond donor-acceptor role of the distal residues in hydroxyl ligand stabilization of Thermobifida fusca truncated hemoglobin
- Source :
- Biochemistry, Biochemistry, American Chemical Society, 2014, pp.9. ⟨10.1021/bi501132a⟩
- Publication Year :
- 2014
-
Abstract
- The unique architecture of the active site of Thermobifida fusca truncated hemoglobin (Tf-trHb) and other globins belonging to the same family has stimulated extensive studies aimed at understanding the interplay between iron-bound ligands and distal amino acids. The behavior of the heme-bound hydroxyl, in particular, has generated much interest in view of the relationships between the spin-state equilibrium of the ferric iron atom and hydrogen-bonding capabilities (as either acceptor or donor) of the OH− group itself. The present investigation offers a detailed molecular dynamics and spectroscopic picture of the hydroxyl complexes of the WT protein and a combinatorial set of mutants, in which the distal polar residues, TrpG8, TyrCD1, and TyrB10, have been singly, doubly, or triply replaced by a Phe residue. Each mutant is characterized by a complex interplay of interactions in which the hydroxyl ligand may act both as a H-bond donor or acceptor. The resonance Raman stretching frequencies of the Fe−OH moiety, together with electron paramagnetic resonance spectra and MD simulations on each mutant, have enabled the identification of specific contributions to the unique ligand-inclusive H-bond network typical of this globin family. Fil: Nicoletti, Francesco P.. Universita Degli Studi Di Firenze; Italia Fil: Bustamante, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Droghetti, Enrica. Universita Degli Studi Di Firenze; Italia Fil: Howes, Barry D.. Universita Degli Studi Di Firenze; Italia Fil: Fittipaldi, Maria. Universita Degli Studi Di Firenze; Italia Fil: Bonamore, Alessandra. Universita Di Roma; Italia Fil: Baiocco, Paola. Italian Institute of Technology; Italia Fil: Feis, Alessandro. Universita Degli Studi Di Firenze; Italia Fil: Boffi, Alberto. Universita Di Roma; Italia Fil: Estrin, Dario Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Smulevich, Giulietta. Universita Degli Studi Di Firenze; Italia
- Subjects :
- SPIN-STATE EQUILIBRIA
Models, Molecular
Hemeprotein
Heme binding
Stereochemistry
Metal Binding Site
Heme
Molecular Dynamics Simulation
Ligands
Spectrum Analysis, Raman
Biochemistry
chemistry.chemical_compound
Bacterial Proteins
Actinomycetales
SPECTRA
[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
Globin
HYDROXYL LIGAND STABILIZATION
HEME-PROTEINS
METALLOPROTEINS
TRUNCATED HEMOGLOBIN
Binding Sites
biology
Hydrogen bond
Chemistry
Ligand
ACTIVE-SITE
RESONANCE RAMAN
Protein Stability
Otras Ciencias Químicas
Ciencias Químicas
Electron Spin Resonance Spectroscopy
Active site
MOLECULAR DYNAMIC SIMULATIONS
Truncated Hemoglobins
HORSERADISH-PEROXIDASE
METMYOGLOBIN
Hydrogen Bonding
Hydrogen-Ion Concentration
ELECTRON-PARAMAGNETIC RESONANCE, SPIN-STATE EQUILIBRIA, HEME-PROTEINS, HORSERADISH-PEROXIDASE, ACTIVE-SITE, SPECTRA, COMPLEXES, METALLOPROTEINS, METHEMOGLOBIN, METMYOGLOBIN
Recombinant Proteins
ELECTRON-PARAMAGNETIC RESONANCE
biology.protein
Mutagenesis, Site-Directed
COMPLEXES
CIENCIAS NATURALES Y EXACTAS
METHEMOGLOBIN
Subjects
Details
- ISSN :
- 15204995 and 00062960
- Volume :
- 53
- Issue :
- 51
- Database :
- OpenAIRE
- Journal :
- Biochemistry
- Accession number :
- edsair.doi.dedup.....bb4a9072bc5b08e88d8e66bb0dd3d95e
- Full Text :
- https://doi.org/10.1021/bi501132a⟩