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Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes

Respiratory electron transport complexes are organized as individual entities or combined as large supercomplexes (SC). Gram-negative bacteria deploy a mitochondrial-like cytochrome (cyt) bc(1) (Complex III, CIII(2)), and may have specific cbb(3)-type cyt c oxidases (Complex IV, CIV) instead of the...

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Autores principales: Steimle, Stefan, van Eeuwen, Trevor, Ozturk, Yavuz, Kim, Hee Jong, Braitbard, Merav, Selamoglu, Nur, Garcia, Benjamin A., Schneidman-Duhovny, Dina, Murakami, Kenji, Daldal, Fevzi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876108/
https://www.ncbi.nlm.nih.gov/pubmed/33568648
http://dx.doi.org/10.1038/s41467-021-21051-4
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author Steimle, Stefan
van Eeuwen, Trevor
Ozturk, Yavuz
Kim, Hee Jong
Braitbard, Merav
Selamoglu, Nur
Garcia, Benjamin A.
Schneidman-Duhovny, Dina
Murakami, Kenji
Daldal, Fevzi
author_facet Steimle, Stefan
van Eeuwen, Trevor
Ozturk, Yavuz
Kim, Hee Jong
Braitbard, Merav
Selamoglu, Nur
Garcia, Benjamin A.
Schneidman-Duhovny, Dina
Murakami, Kenji
Daldal, Fevzi
author_sort Steimle, Stefan
collection PubMed
description Respiratory electron transport complexes are organized as individual entities or combined as large supercomplexes (SC). Gram-negative bacteria deploy a mitochondrial-like cytochrome (cyt) bc(1) (Complex III, CIII(2)), and may have specific cbb(3)-type cyt c oxidases (Complex IV, CIV) instead of the canonical aa(3)-type CIV. Electron transfer between these complexes is mediated by soluble (c(2)) and membrane-anchored (c(y)) cyts. Here, we report the structure of an engineered bc(1)-cbb(3) type SC (CIII(2)CIV, 5.2 Å resolution) and three conformers of native CIII(2) (3.3 Å resolution). The SC is active in vivo and in vitro, contains all catalytic subunits and cofactors, and two extra transmembrane helices attributed to cyt c(y) and the assembly factor CcoH. The cyt c(y) is integral to SC, its cyt domain is mobile and it conveys electrons to CIV differently than cyt c(2). The successful production of a native-like functional SC and determination of its structure illustrate the characteristics of membrane-confined and membrane-external respiratory electron transport pathways in Gram-negative bacteria.
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spelling pubmed-78761082021-02-24 Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes Steimle, Stefan van Eeuwen, Trevor Ozturk, Yavuz Kim, Hee Jong Braitbard, Merav Selamoglu, Nur Garcia, Benjamin A. Schneidman-Duhovny, Dina Murakami, Kenji Daldal, Fevzi Nat Commun Article Respiratory electron transport complexes are organized as individual entities or combined as large supercomplexes (SC). Gram-negative bacteria deploy a mitochondrial-like cytochrome (cyt) bc(1) (Complex III, CIII(2)), and may have specific cbb(3)-type cyt c oxidases (Complex IV, CIV) instead of the canonical aa(3)-type CIV. Electron transfer between these complexes is mediated by soluble (c(2)) and membrane-anchored (c(y)) cyts. Here, we report the structure of an engineered bc(1)-cbb(3) type SC (CIII(2)CIV, 5.2 Å resolution) and three conformers of native CIII(2) (3.3 Å resolution). The SC is active in vivo and in vitro, contains all catalytic subunits and cofactors, and two extra transmembrane helices attributed to cyt c(y) and the assembly factor CcoH. The cyt c(y) is integral to SC, its cyt domain is mobile and it conveys electrons to CIV differently than cyt c(2). The successful production of a native-like functional SC and determination of its structure illustrate the characteristics of membrane-confined and membrane-external respiratory electron transport pathways in Gram-negative bacteria. Nature Publishing Group UK 2021-02-10 /pmc/articles/PMC7876108/ /pubmed/33568648 http://dx.doi.org/10.1038/s41467-021-21051-4 Text en © The Author(s) 2021 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
Steimle, Stefan
van Eeuwen, Trevor
Ozturk, Yavuz
Kim, Hee Jong
Braitbard, Merav
Selamoglu, Nur
Garcia, Benjamin A.
Schneidman-Duhovny, Dina
Murakami, Kenji
Daldal, Fevzi
Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes
title Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes
title_full Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes
title_fullStr Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes
title_full_unstemmed Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes
title_short Cryo-EM structures of engineered active bc(1)-cbb(3) type CIII(2)CIV super-complexes and electronic communication between the complexes
title_sort cryo-em structures of engineered active bc(1)-cbb(3) type ciii(2)civ super-complexes and electronic communication between the complexes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876108/
https://www.ncbi.nlm.nih.gov/pubmed/33568648
http://dx.doi.org/10.1038/s41467-021-21051-4
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