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|Title:||Vibrational resonances and Cu B displacement controlled by proton motion in cytochrome c oxidase||Authors:||Farantos, Stavros C.
|Keywords:||Porphyrins;Cell membranes;Enzymes;Hemoglobin;Molecular dynamics;Phosphatases;Protons;Resonance||Category:||Earth and related Environmental Sciences||Field:||Natural Sciences||Issue Date:||2010||Publisher:||ACS Publications||Source:||Journal of physical chemistry B, 2010, volume 114, issue 2, pages 1136-1143||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||URI:||http://ktisis.cut.ac.cy/handle/10488/6549||ISSN:||15206106||DOI:||10.1021/jp910006k||Collaboration :||Centro Nacional de Supercomputación & Institució Catalana de Recerca i Estudis Avançats (ICREA)
Cyprus University of Technology
Foundation of Research and Technology of Greece
University of Crete
|Rights:||© 2010 American Chemical Society||Type:||Article|
|Appears in Collections:||Άρθρα/Articles|
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