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Cytochrome c Oxidase: Catalytic Cycle and Mechanisms of Proton Pumping-A Discussion
Abstract
Cytochrome c oxidase catalyzes the reduction of molecular oxygen to water, a process in which four electrons, four protons, and one molecule of oxygen are consumed. The reaction is coupled to the pumping of four additional protons across the membrane. According to the currently accepted concept, the pumping of all four protons occurs after the binding of oxygen to the reduced enzyme and is exclusively coupled to the last two electron transfer steps. A careful analysis of the existing data shows that there is no experimental evidence for this paradigm. It is more likely that only three protons are pumped during the second half of the catalytic cycle of cytochrome c oxidase after the reaction with oxygen. In this article a variant of a recent mechanistic model of proton pumping by electrostatic repulsion is discussed. It is based on the electroneutrality principle in a way that in the catalytic cycle each electron transfer to the membrane-embedded electron acceptors is charge-compensated by uptake of one proton. The mechanism takes into account the findings with mutant cytochrome c oxidases and explains the results of many recent experiments, including the effects of hydrogen peroxide.
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Citations
Cited by
Theory of Coupled Electron and Proton Transfer Reactions
Hammes-Schiffer, S., & Stuchebrukhov, A. A. (2010) · Chemical Reviews · doi:10.1021/cr1001436 · Cited by 848
Functional Analogues of Cytochrome c Oxidase, Myoglobin, and Hemoglobin
Collman, J. P., Boulatov, R., Sunderland, C. J., & Fu, L. (2004) · Chemical Reviews · doi:10.1021/cr0206059 · Cited by 685
LAMBERT, A. J., & BRAND, M. D. (2004) · Biochemical Journal · doi:10.1042/bj20040485 · Cited by 470
Structure and mechanism of the aberrant ba3-cytochrome c oxidase from Thermus thermophilus
Soulimane, T. (2000) · The EMBO Journal · doi:10.1093/emboj/19.8.1766 · Cited by 468
Crystal structure of DegP (HtrA) reveals a new protease-chaperone machine
Krojer, T., Garrido-Franco, M., Huber, R., Ehrmann, M., & Clausen, T. (2002) · Nature · doi:10.1038/416455a · Cited by 403
Metadata
- Authors
- Michel, H.
- Venue
- Biochemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 1999-10-30
- Volume
- 38
- Issue
- 46
- Pages
- 15129-15140
- ISSN
- 0006-2960 (ISSN-L)
- 1520-4995
- OpenAlex
- W2157256442
- Cited by
- 248
- References
- 0
- FWCI
- 10.77
- Type
- journal article
- Language
- en
- Open access
- closed
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