Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/3303
DC FieldValueLanguage
dc.contributor.authorFarantos, Stavros C.-
dc.contributor.authorGuallar, Victor-
dc.contributor.authorVarotsis, Constantinos-
dc.contributor.authorDaskalakis, Vangelis-
dc.date.accessioned2013-01-16T13:42:16Zen
dc.date.accessioned2013-05-17T07:13:15Z-
dc.date.accessioned2015-12-08T07:52:52Z-
dc.date.available2013-01-16T13:42:16Zen
dc.date.available2013-05-17T07:13:15Z-
dc.date.available2015-12-08T07:52:52Z-
dc.date.issued2010-01-21-
dc.identifier.citationJournal of physical chemistry B, 2010, vol. 114, no. 2, pp. 1136-1143en_US
dc.identifier.issn15205207-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/3303-
dc.description.abstractCytochrome 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 spectraen_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofThe Journal of Physical Chemistry Ben_US
dc.rights© American Chemical Societyen_US
dc.subjectElectron Transport Complex IVen_US
dc.subjectHemeen_US
dc.subjectHeme a3en_US
dc.titleVibrational resonances and Cu B displacement controlled by proton motion in cytochrome c oxidaseen_US
dc.typeArticleen_US
dc.collaborationCentro Nacional de Supercomputación & Institució Catalana de Recerca i Estudis Avançats (ICREA)en_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationFoundation for Research & Technology-Hellas (F.O.R.T.H.)en_US
dc.collaborationUniversity of Creteen_US
dc.journalsSubscriptionen_US
dc.reviewpeer reviewed-
dc.countryGreeceen_US
dc.countryCyprusen_US
dc.subject.fieldNatural Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1021/jp910006ken_US
dc.dept.handle123456789/77en
dc.relation.issue2en_US
dc.relation.volume114en_US
cut.common.academicyear2009-2010en_US
dc.identifier.spage1136en_US
dc.identifier.epage1143en_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.journal.journalissn1520-5207-
crisitem.journal.publisherAmerican Chemical Society-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.orcid0000-0003-2771-8891-
crisitem.author.orcid0000-0001-8870-0850-
crisitem.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
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