Role of nuclear-encoded subunit Vb in the assembly and stability of cytochrome c oxidase complex: implications in mitochondrial dysfunction and ROS production

Biochem J. 2009 May 27;420(3):439-49. doi: 10.1042/BJ20090214.

Abstract

CcO (cytochrome c oxidase) is a multisubunit bigenomic protein complex which catalyses the last step of the mitochondrial electron transport chain. The nuclear-encoded subunits are thought to have roles either in regulation or in the structural stability of the enzyme. Subunit Vb is a peripheral nuclear-encoded subunit of mammalian CcO that is dramatically reduced under hypoxia. Although it has been shown to contain different ligand-binding sites and undergo modifications, its precise function is not known. In the present study we generated a cell line from RAW 264.7 murine macrophages that has a more than 80% reduced level of Vb. Functional analysis of these cells showed a loss of CcO activity, membrane potential and less ability to generate ATP. Resolution of complexes on blue native gel and two-dimensional electrophoretic analysis showed an accumulation of subcomplexes of CcO and also reduced association with supercomplexes of the electron transfer chain. Furthermore, the mitochondria from CcO Vb knock-down cells generated increased ROS (reactive oxygen species), and the cells were unable to grow on galactose-containing medium. Pulse-chase experiments suggest the role of the CcO Vb subunit in the assembly of the complex. We show for the first time the role of a peripheral, non-transmembrane subunit in the formation as well as function of the terminal CcO complex.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Cell Line
  • Cell Nucleus / genetics
  • Cell Proliferation / drug effects
  • Electron Spin Resonance Spectroscopy
  • Electron Transport
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism*
  • Electrophoresis, Gel, Two-Dimensional
  • Enzyme Stability
  • Galactose / pharmacology
  • Immunoblotting
  • Macrophages / cytology
  • Macrophages / metabolism*
  • Membrane Potential, Mitochondrial / physiology
  • Mice
  • Mitochondria / metabolism*
  • Mitochondria / physiology
  • Oxygen Consumption / physiology
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • RNA, Small Interfering / genetics
  • Reactive Oxygen Species / metabolism*
  • Transfection

Substances

  • Protein Subunits
  • RNA, Small Interfering
  • Reactive Oxygen Species
  • Adenosine Triphosphate
  • COX5B protein, human
  • Electron Transport Complex IV
  • Galactose