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https://hdl.handle.net/20.500.14279/3303
Πεδίο DC | Τιμή | Γλώσσα |
---|---|---|
dc.contributor.author | Farantos, Stavros C. | - |
dc.contributor.author | Guallar, Victor | - |
dc.contributor.author | Varotsis, Constantinos | - |
dc.contributor.author | Daskalakis, Vangelis | - |
dc.date.accessioned | 2013-01-16T13:42:16Z | en |
dc.date.accessioned | 2013-05-17T07:13:15Z | - |
dc.date.accessioned | 2015-12-08T07:52:52Z | - |
dc.date.available | 2013-01-16T13:42:16Z | en |
dc.date.available | 2013-05-17T07:13:15Z | - |
dc.date.available | 2015-12-08T07:52:52Z | - |
dc.date.issued | 2010-01-21 | - |
dc.identifier.citation | Journal of physical chemistry B, 2010, vol. 114, no. 2, pp. 1136-1143 | en_US |
dc.identifier.issn | 15205207 | - |
dc.identifier.uri | https://hdl.handle.net/20.500.14279/3303 | - |
dc.description.abstract | Cytochrome c oxidase (CcO), found in the inner mitochondrial membranes or in many bacteria, catalyzes the four-electron reduction of molecular oxygen to water. Four protons are pumped across the inner mitochondrial membrane through CcO. In this study, quantum mechanics/molecular mechanics and molecular dynamics calculations are used to probe the spectroscopic characteristics of the ferryl intermediates in the aa 3 CcO/O 2 reaction. These highly elaborate calculations, supported by several calculations on smaller model systems, demonstrate the sensitivity of vibrational frequencies on the Coulombic field of heme a 3 and their dependence on the distance of the adjacent Cu B to the heme a 3-Fe atom. This distance seems to be associated with the protonation state of the heme a 3 propionate A, and we propose that it plays a crucial role on the mechanism of action of CcO. In detail, we link proton pumping activity in CcO enzyme (a) to a multiple (1:1:2) resonance among the frequencies of FeIV=O bond stretching, the breathing mode of Histidine 411, and a bending mode of the His411-FeIV=O species (aa 3 from Paracoccus denitrificans numbering) and (b) to Cu B displacement by electrostatic interactions toward the heme a 3 iron. We find that the vibrations of the His411-FeIV=O unit become highly coupled depending on the protonation state of the heme a 3 ring A propionate/Asp399 pair, and we propose a mechanism for the resonance Raman enhancement of the bending mode δ(His411-FeIV=O). Calculations on model systems demonstrate that the position of Cu B in relation to heme a 3 iron-oxo plays a crucial role in regulating that resonance. We also discuss the origin of the coupling between bending, δ(His411- FeIV=O) and v(Fe=O) stretching modes, and the role played by such vibrational coupling interactions or CuB position in controlling functional properties of the enzyme, including electron/proton coupling as well as experimental spectra | en_US |
dc.format | en_US | |
dc.language.iso | en | en_US |
dc.relation.ispartof | The Journal of Physical Chemistry B | en_US |
dc.rights | © American Chemical Society | en_US |
dc.subject | Electron Transport Complex IV | en_US |
dc.subject | Heme | en_US |
dc.subject | Heme a3 | en_US |
dc.title | Vibrational resonances and Cu B displacement controlled by proton motion in cytochrome c oxidase | en_US |
dc.type | Article | en_US |
dc.collaboration | Centro Nacional de Supercomputación & Institució Catalana de Recerca i Estudis Avançats (ICREA) | en_US |
dc.collaboration | Cyprus University of Technology | en_US |
dc.collaboration | Foundation for Research & Technology-Hellas (F.O.R.T.H.) | en_US |
dc.collaboration | University of Crete | en_US |
dc.journals | Subscription | en_US |
dc.review | peer reviewed | - |
dc.country | Greece | en_US |
dc.country | Cyprus | en_US |
dc.subject.field | Natural Sciences | en_US |
dc.publication | Peer Reviewed | en_US |
dc.identifier.doi | 10.1021/jp910006k | en_US |
dc.dept.handle | 123456789/77 | en |
dc.relation.issue | 2 | en_US |
dc.relation.volume | 114 | en_US |
cut.common.academicyear | 2009-2010 | en_US |
dc.identifier.spage | 1136 | en_US |
dc.identifier.epage | 1143 | en_US |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.openairetype | article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
crisitem.journal.journalissn | 1520-5207 | - |
crisitem.journal.publisher | American Chemical Society | - |
crisitem.author.dept | Department of Chemical Engineering | - |
crisitem.author.dept | Department of Chemical Engineering | - |
crisitem.author.faculty | Faculty of Geotechnical Sciences and Environmental Management | - |
crisitem.author.faculty | Faculty of Geotechnical Sciences and Environmental Management | - |
crisitem.author.orcid | 0000-0003-2771-8891 | - |
crisitem.author.orcid | 0000-0001-8870-0850 | - |
crisitem.author.parentorg | Faculty of Geotechnical Sciences and Environmental Management | - |
crisitem.author.parentorg | Faculty of Geotechnical Sciences and Environmental Management | - |
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