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Three-dimensional structure of the apoptosome: Implications for assembly, procaspase-9 binding, and activation

  • Devrim Acehan
  • , Xuejun Jiang
  • , David Gene Morgan
  • , John E. Heuser
  • , Xiaodong Wang
  • , Christopher W. Akey
  • University of Texas at Dallas
  • Boston University
  • Harvard University
  • Washington University St. Louis

Research output: Contribution to journalArticlepeer-review

768 Scopus citations

Abstract

The apoptosome is an Apaf-1 cytochrome c complex that activates procaspase-9. The three-dimensional structure of the apoptosome has been determined at 27 Å resolution, to reveal a wheel-like particle with 7-fold symmetry. Molecular modeling was used to identify the caspase recruitment and WD40 domains within the apoptosome and to infer likely positions of the CED4 homology motif and cytochrome c. This analysis suggests a plausible role for cytochrome c in apoptosome assembly. In a subsequent structure, a noncleavable mutant of procaspase-9 was localized to the central region of the apoptosome. This complex promotes the efficient activation of procaspase-3. Therefore, the cleavage of procaspase-9 is not required to form an active cell death complex.

Original languageEnglish
Pages (from-to)423-432
Number of pages10
JournalMolecular Cell
Volume9
Issue number2
DOIs
StatePublished - 2002

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