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XIAP Is a copper binding protein deregulated in Wilson's disease and other copper toxicosis disorders.

X-linked inhibitor of apoptosis (XIAP), known primarily for its caspase inhibitory properties, has recently been shown to interact with and regulate the levels of COMMD1, a protein associated with a form of canine copper toxicosis. Here, we describe a role for XIAP in copper metabolism. We find that XIAP levels are greatly reduced by intracellular copper accumulation in Wilson's disease and other copper toxicosis disorders and in cells cultured under high copper conditions. Elevated copper levels result in a profound, reversible conformational change in XIAP due to the direct binding of copper to XIAP, which accelerates its degradation and significantly decreases its ability to inhibit caspase-3. This results in a lowering of the apoptotic threshold, sensitizing the cell to apoptosis. These data provide an unsuspected link between copper homeostasis and the regulation of cell death through XIAP and may contribute to the pathophysiology of copper toxicosis disorders.

Pubmed ID: 16543147


  • Mufti AR
  • Burstein E
  • Csomos RA
  • Graf PC
  • Wilkinson JC
  • Dick RD
  • Challa M
  • Son JK
  • Bratton SB
  • Su GL
  • Brewer GJ
  • Jakob U
  • Duckett CS


Molecular cell

Publication Data

March 17, 2006

Associated Grants

  • Agency: NIGMS NIH HHS, Id: GM067827
  • Agency: NCRR NIH HHS, Id: M01-RR00042

Mesh Terms

  • Apoptosis
  • Carrier Proteins
  • Caspase 3
  • Caspases
  • Cell Line
  • Copper
  • Electrophoretic Mobility Shift Assay
  • Hepatolenticular Degeneration
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Models, Biological
  • Protein Conformation
  • Signal Transduction
  • Transfection
  • X-Linked Inhibitor of Apoptosis Protein