Portrait of a killer: the mitochondrial apoptosome emerges from the shadows

Mol Interv. 2003 Feb;3(1):19-26. doi: 10.1124/mi.3.1.19.

Abstract

Apoptosis (programmed cell death) is a physiological process used to eliminate superfluous, damaged, infected, or aged cells in multicellular organisms. During apoptosis the cellular architecture is dismantled from within in a highly controlled fashion. Members of the caspase family of cysteine proteases are responsible for the destructive phase of apoptosis. One major pathway to caspase activation involves the formation of a multisubunit protease activation complex called the apoptosome. The apoptosome is assembled in response to signals that provoke mitochondrial outer membrane permeabilization and the release of cytochrome c into the cytosol. Recent studies indicate that the apoptosome is a wheel-like structure consisting of seven molecules of Apaf-1 and a similar number of caspase-9 dimers. Knowledge of the structure of the apoptosome will likely lead to the design of therapeutic modulators of apoptosis.

Publication types

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

MeSH terms

  • Apoptosis / physiology*
  • Apoptotic Protease-Activating Factor 1
  • Caspase 9
  • Caspases / chemistry*
  • Caspases / metabolism*
  • Cytochrome c Group / physiology*
  • Deoxyadenine Nucleotides / metabolism
  • Dimerization
  • Enzyme Activation
  • Humans
  • Mitochondria / metabolism
  • Mitochondria / physiology*
  • Models, Molecular
  • Proteins / chemistry*
  • Proteins / metabolism*

Substances

  • APAF1 protein, human
  • Apoptotic Protease-Activating Factor 1
  • Cytochrome c Group
  • Deoxyadenine Nucleotides
  • Proteins
  • CASP9 protein, human
  • Caspase 9
  • Caspases
  • 2'-deoxyadenosine triphosphate