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Binding of Natural Inhibitors to Respiratory Complex I

NADH:ubiquinone oxidoreductase (respiratory complex I) is a redox-driven proton pump with a central role in mitochondrial oxidative phosphorylation. The ubiquinone reduction site of complex I is located in the matrix arm of this large protein complex and connected to the membrane via a tunnel. A var...

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Autores principales: Schiller, Jonathan, Zickermann, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503403/
https://www.ncbi.nlm.nih.gov/pubmed/36145309
http://dx.doi.org/10.3390/ph15091088
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author Schiller, Jonathan
Zickermann, Volker
author_facet Schiller, Jonathan
Zickermann, Volker
author_sort Schiller, Jonathan
collection PubMed
description NADH:ubiquinone oxidoreductase (respiratory complex I) is a redox-driven proton pump with a central role in mitochondrial oxidative phosphorylation. The ubiquinone reduction site of complex I is located in the matrix arm of this large protein complex and connected to the membrane via a tunnel. A variety of chemically diverse compounds are known to inhibit ubiquinone reduction by complex I. Rotenone, piericidin A, and annonaceous acetogenins are representatives of complex I inhibitors from biological sources. The structure of complex I is determined at high resolution, and inhibitor binding sites are described in detail. In this review, we summarize the state of knowledge of how natural inhibitors bind in the Q reduction site and the Q access pathway and how their inhibitory mechanisms compare with that of a synthetic anti-cancer agent.
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spelling pubmed-95034032022-09-24 Binding of Natural Inhibitors to Respiratory Complex I Schiller, Jonathan Zickermann, Volker Pharmaceuticals (Basel) Review NADH:ubiquinone oxidoreductase (respiratory complex I) is a redox-driven proton pump with a central role in mitochondrial oxidative phosphorylation. The ubiquinone reduction site of complex I is located in the matrix arm of this large protein complex and connected to the membrane via a tunnel. A variety of chemically diverse compounds are known to inhibit ubiquinone reduction by complex I. Rotenone, piericidin A, and annonaceous acetogenins are representatives of complex I inhibitors from biological sources. The structure of complex I is determined at high resolution, and inhibitor binding sites are described in detail. In this review, we summarize the state of knowledge of how natural inhibitors bind in the Q reduction site and the Q access pathway and how their inhibitory mechanisms compare with that of a synthetic anti-cancer agent. MDPI 2022-08-31 /pmc/articles/PMC9503403/ /pubmed/36145309 http://dx.doi.org/10.3390/ph15091088 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Schiller, Jonathan
Zickermann, Volker
Binding of Natural Inhibitors to Respiratory Complex I
title Binding of Natural Inhibitors to Respiratory Complex I
title_full Binding of Natural Inhibitors to Respiratory Complex I
title_fullStr Binding of Natural Inhibitors to Respiratory Complex I
title_full_unstemmed Binding of Natural Inhibitors to Respiratory Complex I
title_short Binding of Natural Inhibitors to Respiratory Complex I
title_sort binding of natural inhibitors to respiratory complex i
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503403/
https://www.ncbi.nlm.nih.gov/pubmed/36145309
http://dx.doi.org/10.3390/ph15091088
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