The effect of Abeta conformation on the metal affinity and aggregation mechanism studied by circular dichroism spectroscopy

J Biochem. 2006 Apr;139(4):733-40. doi: 10.1093/jb/mvj083.

Abstract

The conformational change and associated aggregation of beta amyloid (Abeta) with or without metals is the main cause of Alzheimer's disease (AD). In order to further understand the effects of Abeta and its associated metals on the aggregation mechanism, the influence of Abeta conformation on the metal affinity and aggregation was investigated using circular dichroism (CD) spectroscopy. The Abeta conformation is dependent on pH and trifluoroethanol (TFE). The binding of metals to Abeta was found to be dependent on the Abeta conformation. The aggregation induced by Abeta itself or its associated metals is completely diminished for Abeta in 40% TFE. Only in 5% and 25% TFE can Abeta undergo an alpha-helix to beta-sheet aggregation, which involve a three-state mechanism for the metal-free state, and a two-state transition for the metal-bound state, respectively. The aggregation-inducing activity of metals is in the order, Cu2+ > Fe3+ > or = Al3+ > Zn2+.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid / chemistry
  • Amyloid / metabolism
  • Amyloid beta-Peptides / chemistry*
  • Amyloid beta-Peptides / metabolism
  • Binding, Competitive
  • Circular Dichroism / methods*
  • Copper / chemistry
  • Copper / metabolism
  • Hydrogen-Ion Concentration
  • Kinetics
  • Macromolecular Substances / chemistry
  • Metals / chemistry*
  • Metals / metabolism
  • Peptide Fragments / metabolism
  • Protein Binding
  • Protein Conformation / drug effects
  • Protein Structure, Secondary
  • Trifluoroethanol / pharmacology
  • Zinc / chemistry
  • Zinc / metabolism

Substances

  • Amyloid
  • Amyloid beta-Peptides
  • Macromolecular Substances
  • Metals
  • Peptide Fragments
  • Trifluoroethanol
  • Copper
  • Zinc