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Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance

Respiratory chains are crucial for cellular energy conversion and consist of multi‐subunit complexes that can assemble into supercomplexes. These structures have been intensively characterized in various organisms, but their physiological roles remain unclear. Here, we elucidate their function by le...

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Autores principales: Berndtsson, Jens, Kohler, Andreas, Rathore, Sorbhi, Marin‐Buera, Lorena, Dawitz, Hannah, Diessl, Jutta, Kohler, Verena, Barrientos, Antoni, Büttner, Sabrina, Fontanesi, Flavia, Ott, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726804/
https://www.ncbi.nlm.nih.gov/pubmed/33016568
http://dx.doi.org/10.15252/embr.202051015
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author Berndtsson, Jens
Kohler, Andreas
Rathore, Sorbhi
Marin‐Buera, Lorena
Dawitz, Hannah
Diessl, Jutta
Kohler, Verena
Barrientos, Antoni
Büttner, Sabrina
Fontanesi, Flavia
Ott, Martin
author_facet Berndtsson, Jens
Kohler, Andreas
Rathore, Sorbhi
Marin‐Buera, Lorena
Dawitz, Hannah
Diessl, Jutta
Kohler, Verena
Barrientos, Antoni
Büttner, Sabrina
Fontanesi, Flavia
Ott, Martin
author_sort Berndtsson, Jens
collection PubMed
description Respiratory chains are crucial for cellular energy conversion and consist of multi‐subunit complexes that can assemble into supercomplexes. These structures have been intensively characterized in various organisms, but their physiological roles remain unclear. Here, we elucidate their function by leveraging a high‐resolution structural model of yeast respiratory supercomplexes that allowed us to inhibit supercomplex formation by mutation of key residues in the interaction interface. Analyses of a mutant defective in supercomplex formation, which still contains fully functional individual complexes, show that the lack of supercomplex assembly delays the diffusion of cytochrome c between the separated complexes, thus reducing electron transfer efficiency. Consequently, competitive cellular fitness is severely reduced in the absence of supercomplex formation and can be restored by overexpression of cytochrome c. In sum, our results establish how respiratory supercomplexes increase the efficiency of cellular energy conversion, thereby providing an evolutionary advantage for aerobic organisms.
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spelling pubmed-77268042020-12-13 Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance Berndtsson, Jens Kohler, Andreas Rathore, Sorbhi Marin‐Buera, Lorena Dawitz, Hannah Diessl, Jutta Kohler, Verena Barrientos, Antoni Büttner, Sabrina Fontanesi, Flavia Ott, Martin EMBO Rep Reports Respiratory chains are crucial for cellular energy conversion and consist of multi‐subunit complexes that can assemble into supercomplexes. These structures have been intensively characterized in various organisms, but their physiological roles remain unclear. Here, we elucidate their function by leveraging a high‐resolution structural model of yeast respiratory supercomplexes that allowed us to inhibit supercomplex formation by mutation of key residues in the interaction interface. Analyses of a mutant defective in supercomplex formation, which still contains fully functional individual complexes, show that the lack of supercomplex assembly delays the diffusion of cytochrome c between the separated complexes, thus reducing electron transfer efficiency. Consequently, competitive cellular fitness is severely reduced in the absence of supercomplex formation and can be restored by overexpression of cytochrome c. In sum, our results establish how respiratory supercomplexes increase the efficiency of cellular energy conversion, thereby providing an evolutionary advantage for aerobic organisms. John Wiley and Sons Inc. 2020-10-05 2020-12-03 /pmc/articles/PMC7726804/ /pubmed/33016568 http://dx.doi.org/10.15252/embr.202051015 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reports
Berndtsson, Jens
Kohler, Andreas
Rathore, Sorbhi
Marin‐Buera, Lorena
Dawitz, Hannah
Diessl, Jutta
Kohler, Verena
Barrientos, Antoni
Büttner, Sabrina
Fontanesi, Flavia
Ott, Martin
Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance
title Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance
title_full Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance
title_fullStr Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance
title_full_unstemmed Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance
title_short Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance
title_sort respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726804/
https://www.ncbi.nlm.nih.gov/pubmed/33016568
http://dx.doi.org/10.15252/embr.202051015
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