The architecture of respiratory supercomplexes
Open accessAbstract
Mitochondrial electron transport chain complexes are organized into supercomplexes responsible for carrying out cellular respiration. Here we present three architectures of mammalian (ovine) supercomplexes determined by cryo-electron microscopy. We identify two distinct arrangements of supercomplex CICIII 2 CIV (the respirasome)-a major 'tight' form and a minor 'loose' form (resolved at the resolution of 5.8 Å and 6.7 Å, respectively), which may represent different stages in supercomplex assembly or disassembly. We have also determined an architecture of supercomplex CICIII 2 at 7.8 Å resolution. All observed density can be attributed to the known 80 subunits of the individual complexes, including 132 transmembrane helices. The individual complexes form tight interactions that vary between the architectures, with complex IV subunit COX7a switching contact from complex III to complex I. The arrangement of active sites within the supercomplex may help control reactive oxygen species production. To our knowledge, these are the first complete architectures of the dominant, physiologically relevant state of the electron transport chain.
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Many mitochondrial proteins must be assembled into large, multi-subunit structures, some of which form supercomplexes that are essential for mitochondrial energy metabolism.
“many must be assembled into large, multi-subunit structures, some of which form “supercomplexes” [39] that are essential for mitochondrial energy metabolism [40]”
From Neuronal Apolipoprotein E4 Expression Results in Proteome-Wide Alterations and Compromises Bioenergetic Capacity by Disrupting Mitochondrial Function (2019) · cites this paper as [39]
COX7a has a critical role in stabilizing complexes III and IV.
“For example, COX7a has a critical role in stabilizing complexes III and IV [39] and is significantly decreased in apoE4-expressing neurons.”
From Neuronal Apolipoprotein E4 Expression Results in Proteome-Wide Alterations and Compromises Bioenergetic Capacity by Disrupting Mitochondrial Function (2019) · cites this paper as [39]
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The Phyre2 web portal for protein modeling, prediction and analysis
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Structure of the Hydrophilic Domain of Respiratory Complex I from <i>Thermus thermophilus</i>
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Self-citationSystems proteomics of liver mitochondria function
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- Authors
- Letts, J. A., Fiedorczuk, K., & Sazanov, L. A.
- Affiliations
- Institute of Science and Technology Austria (AT)
- Corresponding author
- Sazanov, Leonid A.
- Venue
- Nature
- Published
- 2016-09
- Volume
- 537
- Issue
- 7622
- Pages
- 644-648
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2523288451
- Cited by
- 490
- References
- 3
- Citations by year
- 2026: 34 · 2025: 27 · 2024: 37 · 2023: 40 · 2022: 33 · 2021: 75 · 2020: 67 · 2019: 48 · 2018: 71 · 2017: 51 · 2016: 7
- FWCI
- 25.34
- Type
- journal article
- Language
- en
- Open access
- green
- zenodo.org
- Licence
- other-oa
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, other-oa)
- Funders
- Medical Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Advanced Electron Microscopy Techniques and Applications
- Physical Sciences › Materials Science › Materials Chemistry › Enzyme Structure and Function
- Keywords
- respirasome, respiratory supercomplexes, mitochondrial electron transport chain, complex I, cytochrome c oxidase, reactive oxygen species, cellular respiration
- MeSH terms
- Animals, Binding Sites, Electron Transport Complex IV, Electron Transport, Heart, Mitochondria, Models, Molecular, Protein Binding, Protein Conformation, Sheep, Electron Transport Complex III, Reactive Oxygen Species, Protein Structure, Secondary, Cell Respiration, Catalytic Domain, Cryoelectron Microscopy, Protein Subunits, Electron Transport Complex I, Protein Stability
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