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  Using cryo-EM to understand the assembly pathway of respiratory complex I

Laube, E., Schiller, J., Zickermann, V., & Vonck, J. (2024). Using cryo-EM to understand the assembly pathway of respiratory complex I. Acta Crystallographica Section D: Structural Biology. doi:10.1107/S205979832400086X.

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 Creators:
Laube, Eike1, Author                 
Schiller, Jonathan2, 3, Author
Zickermann, Volker2, 3, Author
Vonck, Janet1, Author                 
Affiliations:
1Department of Structural Biology, Max Planck Institute of Biophysics, Max Planck Society, ou_2068291              
2Institute of Biochemistry II, University Hospital, Goethe University, Frankfurt am Main, Germany, ou_persistent22              
3Centre for Biomolecular Magnetic Resonance, Institute for Biophysical Chemistry, Goethe University, Frankfurt am Main, Germany, ou_persistent22              

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Free keywords: assembly factors, complex I assembly, proton-pumping NADH ubiquinone oxidoreductase, respiratory complex I, single-particle cryo-EM
 Abstract: Complex I (proton-pumping NADH:ubiquinone oxidoreductase) is the first component of the mitochondrial respiratory chain. In recent years, high-resolution cryo-EM studies of complex I from various species have greatly enhanced the understanding of the structure and function of this important membrane-protein complex. Less well studied is the structural basis of complex I biogenesis. The assembly of this complex of more than 40 subunits, encoded by nuclear or mitochondrial DNA, is an intricate process that requires at least 20 different assembly factors in humans. These are proteins that are transiently associated with building blocks of the complex and are involved in the assembly process, but are not part of mature complex I. Although the assembly pathways have been studied extensively, there is limited information on the structure and molecular function of the assembly factors. Here, the insights that have been gained into the assembly process using cryo-EM are reviewed.

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Language(s): eng - English
 Dates: 2023-11-102024-01-232024-03-01
 Publication Status: Issued
 Pages: 15
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1107/S205979832400086X
BibTex Citekey: laube_using_2024
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Title: Acta Crystallographica Section D: Structural Biology
  Abbreviation : Acta Cryst. D
Source Genre: Journal
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Publ. Info: Chester, England : International Union of Crystallography
Pages: - Volume / Issue: - Sequence Number: - Start / End Page: - Identifier: ISSN: 2059-7983
CoNE: https://pure.mpg.de/cone/journals/resource/2059-7983