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H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I
NADH:ubiquinone oxidoreductase, respiratory complex I, plays a major role in cellular energy metabolism by coupling electron transfer with proton translocation. Electron transfer is catalyzed by a flavin mononucleotide and a series of iron-sulfur (Fe/S) clusters. As a by-product of the reaction, the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175503/ https://www.ncbi.nlm.nih.gov/pubmed/37169846 http://dx.doi.org/10.1038/s41598-023-34821-5 |
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author | Strotmann, Lisa Harter, Caroline Gerasimova, Tatjana Ritter, Kevin Jessen, Henning J. Wohlwend, Daniel Friedrich, Thorsten |
author_facet | Strotmann, Lisa Harter, Caroline Gerasimova, Tatjana Ritter, Kevin Jessen, Henning J. Wohlwend, Daniel Friedrich, Thorsten |
author_sort | Strotmann, Lisa |
collection | PubMed |
description | NADH:ubiquinone oxidoreductase, respiratory complex I, plays a major role in cellular energy metabolism by coupling electron transfer with proton translocation. Electron transfer is catalyzed by a flavin mononucleotide and a series of iron-sulfur (Fe/S) clusters. As a by-product of the reaction, the reduced flavin generates reactive oxygen species (ROS). It was suggested that the ROS generated by the respiratory chain in general could damage the Fe/S clusters of the complex. Here, we show that the binuclear Fe/S cluster N1b is specifically damaged by H(2)O(2), however, only at high concentrations. But under the same conditions, the activity of the complex is hardly affected, since N1b can be easily bypassed during electron transfer. |
format | Online Article Text |
id | pubmed-10175503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101755032023-05-13 H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I Strotmann, Lisa Harter, Caroline Gerasimova, Tatjana Ritter, Kevin Jessen, Henning J. Wohlwend, Daniel Friedrich, Thorsten Sci Rep Article NADH:ubiquinone oxidoreductase, respiratory complex I, plays a major role in cellular energy metabolism by coupling electron transfer with proton translocation. Electron transfer is catalyzed by a flavin mononucleotide and a series of iron-sulfur (Fe/S) clusters. As a by-product of the reaction, the reduced flavin generates reactive oxygen species (ROS). It was suggested that the ROS generated by the respiratory chain in general could damage the Fe/S clusters of the complex. Here, we show that the binuclear Fe/S cluster N1b is specifically damaged by H(2)O(2), however, only at high concentrations. But under the same conditions, the activity of the complex is hardly affected, since N1b can be easily bypassed during electron transfer. Nature Publishing Group UK 2023-05-11 /pmc/articles/PMC10175503/ /pubmed/37169846 http://dx.doi.org/10.1038/s41598-023-34821-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Strotmann, Lisa Harter, Caroline Gerasimova, Tatjana Ritter, Kevin Jessen, Henning J. Wohlwend, Daniel Friedrich, Thorsten H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I |
title | H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I |
title_full | H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I |
title_fullStr | H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I |
title_full_unstemmed | H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I |
title_short | H(2)O(2) selectively damages the binuclear iron-sulfur cluster N1b of respiratory complex I |
title_sort | h(2)o(2) selectively damages the binuclear iron-sulfur cluster n1b of respiratory complex i |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175503/ https://www.ncbi.nlm.nih.gov/pubmed/37169846 http://dx.doi.org/10.1038/s41598-023-34821-5 |
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