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Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential
The respiratory chain in mitochondria is composed of membrane-bound proteins that couple electron transfer to proton translocation across the inner membrane. These charge-transfer reactions are regulated by the proton electrochemical gradient that is generated and maintained by the transmembrane cha...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085328/ https://www.ncbi.nlm.nih.gov/pubmed/30093670 http://dx.doi.org/10.1038/s41467-018-05615-5 |
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author | Björck, Markus L. Brzezinski, Peter |
author_facet | Björck, Markus L. Brzezinski, Peter |
author_sort | Björck, Markus L. |
collection | PubMed |
description | The respiratory chain in mitochondria is composed of membrane-bound proteins that couple electron transfer to proton translocation across the inner membrane. These charge-transfer reactions are regulated by the proton electrochemical gradient that is generated and maintained by the transmembrane charge transfer. Here, we investigate this feedback mechanism in cytochrome c oxidase in intact inner mitochondrial membranes upon generation of an electrochemical potential by hydrolysis of ATP. The data indicate that a reaction step that involves proton uptake to the catalytic site and presumably proton translocation is impaired by the potential, but electron transfer is not affected. These results define the order of electron and proton-transfer reactions and suggest that the proton pump is regulated by the transmembrane electrochemical gradient through control of internal proton transfer rather than by control of electron transfer. |
format | Online Article Text |
id | pubmed-6085328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60853282018-08-13 Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential Björck, Markus L. Brzezinski, Peter Nat Commun Article The respiratory chain in mitochondria is composed of membrane-bound proteins that couple electron transfer to proton translocation across the inner membrane. These charge-transfer reactions are regulated by the proton electrochemical gradient that is generated and maintained by the transmembrane charge transfer. Here, we investigate this feedback mechanism in cytochrome c oxidase in intact inner mitochondrial membranes upon generation of an electrochemical potential by hydrolysis of ATP. The data indicate that a reaction step that involves proton uptake to the catalytic site and presumably proton translocation is impaired by the potential, but electron transfer is not affected. These results define the order of electron and proton-transfer reactions and suggest that the proton pump is regulated by the transmembrane electrochemical gradient through control of internal proton transfer rather than by control of electron transfer. Nature Publishing Group UK 2018-08-09 /pmc/articles/PMC6085328/ /pubmed/30093670 http://dx.doi.org/10.1038/s41467-018-05615-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Björck, Markus L. Brzezinski, Peter Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential |
title | Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential |
title_full | Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential |
title_fullStr | Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential |
title_full_unstemmed | Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential |
title_short | Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential |
title_sort | control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085328/ https://www.ncbi.nlm.nih.gov/pubmed/30093670 http://dx.doi.org/10.1038/s41467-018-05615-5 |
work_keys_str_mv | AT bjorckmarkusl controloftransmembranechargetransferincytochromecoxidasebythemembranepotential AT brzezinskipeter controloftransmembranechargetransferincytochromecoxidasebythemembranepotential |