Respiratory complex I - Mechanistic insights and advances in structure determination

Biochim Biophys Acta Bioenerg. 2020 Mar 1;1861(3):148153. doi: 10.1016/j.bbabio.2020.148153. Epub 2020 Jan 11.

Abstract

Complex I is the largest and most intricate redox-driven proton pump of the respiratory chain. The structure of bacterial and mitochondrial complex I has been determined by X-ray crystallography and cryo-EM at increasing resolution. The recent cryo-EM structures of the complex I-like NDH complex and membrane bound hydrogenase open a new and more comprehensive perspective on the complex I superfamily. Functional studies and molecular modeling approaches have greatly advanced our understanding of the catalytic cycle of complex I. However, the molecular mechanism by which energy is extracted from the redox reaction and utilized to drive proton translocation is unresolved and a matter of ongoing debate. Here, we review progress in structure determination and functional characterization of complex I and discuss current mechanistic models.

Keywords: Membrane bound hydrogenase; Mitochondria; NADH:Ubiquinone oxidoreductase; Oxidative phosphorylation; Redox-linked proton translocation; Respiratory chain.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Electron Transport Complex I / chemistry*
  • Electron Transport Complex I / metabolism
  • Hydrophobic and Hydrophilic Interactions
  • Oxidation-Reduction
  • Protein Subunits / chemistry
  • Protein Subunits / metabolism
  • Protons
  • Ubiquinone / chemistry
  • Ubiquinone / metabolism

Substances

  • Protein Subunits
  • Protons
  • Ubiquinone
  • Electron Transport Complex I