Copper-dependent Inhibition of Human Cytochrome C Oxidase by a Dimeric Conformer of amyloid-beta1-42

J Neurosci. 2005 Jan 19;25(3):672-9. doi: 10.1523/JNEUROSCI.4276-04.2005.

Abstract

In studies of Alzheimer's disease pathogenesis there is an increasing focus on mechanisms of intracellular amyloid-beta (Abeta) generation and toxicity. Here we investigated the inhibitory potential of the 42 amino acid Abeta peptide (Abeta1-42) on activity of electron transport chain enzyme complexes in human mitochondria. We found that synthetic Abeta1-42 specifically inhibited the terminal complex cytochrome c oxidase (COX) in a dose-dependent manner that was dependent on the presence of Cu2+ and specific "aging" of the Abeta1-42 solution. Maximal COX inhibition occurred when using Abeta1-42 solutions aged for 3-6 h at 30 degrees C. The level of Abeta1-42-mediated COX inhibition increased with aging time up to approximately 6 h and then declined progressively with continued aging to 48 h. Photo-induced cross-linking of unmodified proteins followed by SDS-PAGE analysis revealed dimeric Abeta as the only Abeta species to provide significant temporal correlation with the observed COX inhibition. Analysis of brain and liver from an Alzheimer's model mouse (Tg2576) revealed abundant Abeta immunoreactivity within the brain mitochondria fraction. Our data indicate that endogenous Abeta is associated with brain mitochondria and that Abeta1-42, possibly in its dimeric conformation, is a potent inhibitor of COX, but only when in the presence of Cu2+. We conclude that Cu2+-dependent Abeta-mediated inhibition of COX may be an important contributor to the neurodegeneration process in Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Peptides / chemistry
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Peptides / physiology*
  • Animals
  • Brain / metabolism
  • Cells, Cultured
  • Copper / physiology*
  • Electron Transport Complex IV / antagonists & inhibitors*
  • Humans
  • Mice
  • Mice, Transgenic
  • Mitochondria / metabolism
  • Mitochondria, Liver / metabolism
  • Multiprotein Complexes
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Peptide Fragments / physiology*
  • Time Factors

Substances

  • Amyloid beta-Peptides
  • Multiprotein Complexes
  • Peptide Fragments
  • amyloid beta-protein (1-42)
  • Copper
  • Electron Transport Complex IV