Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783620958220713984 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7726804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT berndtssonjens respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT kohlerandreas respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT rathoresorbhi respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT marinbueralorena respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT dawitzhannah respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT diessljutta respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT kohlerverena respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT barrientosantoni respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT buttnersabrina respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT fontanesiflavia respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance AT ottmartin respiratorysupercomplexesenhanceelectrontransportbydecreasingcytochromecdiffusiondistance |