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High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease
Respiratory complex I is a redox-driven proton pump, accounting for a large part of the electrochemical gradient that powers mitochondrial adenosine triphosphate synthesis. Complex I dysfunction is associated with severe human diseases. Assembly of the one-megadalton complex I in the inner mitochond...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905873/ https://www.ncbi.nlm.nih.gov/pubmed/31844670 http://dx.doi.org/10.1126/sciadv.aax9484 |
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author | Parey, Kristian Haapanen, Outi Sharma, Vivek Köfeler, Harald Züllig, Thomas Prinz, Simone Siegmund, Karin Wittig, Ilka Mills, Deryck J. Vonck, Janet Kühlbrandt, Werner Zickermann, Volker |
author_facet | Parey, Kristian Haapanen, Outi Sharma, Vivek Köfeler, Harald Züllig, Thomas Prinz, Simone Siegmund, Karin Wittig, Ilka Mills, Deryck J. Vonck, Janet Kühlbrandt, Werner Zickermann, Volker |
author_sort | Parey, Kristian |
collection | PubMed |
description | Respiratory complex I is a redox-driven proton pump, accounting for a large part of the electrochemical gradient that powers mitochondrial adenosine triphosphate synthesis. Complex I dysfunction is associated with severe human diseases. Assembly of the one-megadalton complex I in the inner mitochondrial membrane requires assembly factors and chaperones. We have determined the structure of complex I from the aerobic yeast Yarrowia lipolytica by electron cryo-microscopy at 3.2-Å resolution. A ubiquinone molecule was identified in the access path to the active site. The electron cryo-microscopy structure indicated an unusual lipid-protein arrangement at the junction of membrane and matrix arms that was confirmed by molecular simulations. The structure of a complex I mutant and an assembly intermediate provide detailed molecular insights into the cause of a hereditary complex I–linked disease and complex I assembly in the inner mitochondrial membrane. |
format | Online Article Text |
id | pubmed-6905873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69058732019-12-16 High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease Parey, Kristian Haapanen, Outi Sharma, Vivek Köfeler, Harald Züllig, Thomas Prinz, Simone Siegmund, Karin Wittig, Ilka Mills, Deryck J. Vonck, Janet Kühlbrandt, Werner Zickermann, Volker Sci Adv Research Articles Respiratory complex I is a redox-driven proton pump, accounting for a large part of the electrochemical gradient that powers mitochondrial adenosine triphosphate synthesis. Complex I dysfunction is associated with severe human diseases. Assembly of the one-megadalton complex I in the inner mitochondrial membrane requires assembly factors and chaperones. We have determined the structure of complex I from the aerobic yeast Yarrowia lipolytica by electron cryo-microscopy at 3.2-Å resolution. A ubiquinone molecule was identified in the access path to the active site. The electron cryo-microscopy structure indicated an unusual lipid-protein arrangement at the junction of membrane and matrix arms that was confirmed by molecular simulations. The structure of a complex I mutant and an assembly intermediate provide detailed molecular insights into the cause of a hereditary complex I–linked disease and complex I assembly in the inner mitochondrial membrane. American Association for the Advancement of Science 2019-12-11 /pmc/articles/PMC6905873/ /pubmed/31844670 http://dx.doi.org/10.1126/sciadv.aax9484 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Parey, Kristian Haapanen, Outi Sharma, Vivek Köfeler, Harald Züllig, Thomas Prinz, Simone Siegmund, Karin Wittig, Ilka Mills, Deryck J. Vonck, Janet Kühlbrandt, Werner Zickermann, Volker High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease |
title | High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease |
title_full | High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease |
title_fullStr | High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease |
title_full_unstemmed | High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease |
title_short | High-resolution cryo-EM structures of respiratory complex I: Mechanism, assembly, and disease |
title_sort | high-resolution cryo-em structures of respiratory complex i: mechanism, assembly, and disease |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905873/ https://www.ncbi.nlm.nih.gov/pubmed/31844670 http://dx.doi.org/10.1126/sciadv.aax9484 |
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