Chemically synthesized human survivin does not inhibit caspase-3

Protein Sci. 2008 Sep;17(9):1624-9. doi: 10.1110/ps.036145.108. Epub 2008 Jun 6.

Abstract

Survivin is a member of the inhibitor of apoptosis protein (IAP) family that blocks cell death by inhibiting the caspase activation pathways. Overexpressed in all common human neoplasms but undetectable in most normal adult tissues, survivin confers tumor resistance to apoptosis and represents an ideal molecular target for therapeutic intervention. How survivin blocks apoptosis, however, has been a subject of intense debate, as evidenced by conflicting reports regarding whether or not survivin can directly bind and inactivate effector caspases. We chemically synthesized large amounts of highly pure human survivin of 142 amino acid residues using native chemical ligation and functionally compared synthetic survivin and a recombinant XIAP--the most intensively studied member of the IAP family. Inhibition assays showed that, while caspase-3 could be effectively inhibited by XIAP, survivin had no detectable inhibitory activity against the enzyme, even at concentrations several thousand-fold higher than XIAP. Our finding supports the premise that survivin does not directly inhibit effector caspases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Buffers
  • Caspase 3 / analysis
  • Caspase 3 / metabolism*
  • Cell Death / drug effects
  • Dimerization
  • Dose-Response Relationship, Drug
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Inhibitor of Apoptosis Proteins / genetics
  • Inhibitor of Apoptosis Proteins / metabolism*
  • Inhibitor of Apoptosis Proteins / pharmacology
  • Microtubule-Associated Proteins / chemical synthesis*
  • Microtubule-Associated Proteins / chemistry
  • Microtubule-Associated Proteins / isolation & purification
  • Microtubule-Associated Proteins / metabolism*
  • Microtubule-Associated Proteins / pharmacology
  • Molecular Sequence Data
  • Molecular Weight
  • Neoplasm Proteins / chemical synthesis*
  • Neoplasm Proteins / chemistry
  • Neoplasm Proteins / isolation & purification
  • Neoplasm Proteins / metabolism*
  • Neoplasm Proteins / pharmacology
  • Peptide Fragments / chemical synthesis*
  • Peptide Fragments / chemistry
  • Protein Conformation
  • Protein Folding
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Solutions / chemistry
  • Survivin
  • Water / chemistry
  • Zinc / chemistry

Substances

  • BIRC5 protein, human
  • Buffers
  • Enzyme Inhibitors
  • Inhibitor of Apoptosis Proteins
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Peptide Fragments
  • Recombinant Proteins
  • Solutions
  • Survivin
  • Water
  • Caspase 3
  • Zinc