Minimal Zn(2+) binding site of amyloid-β

Biophys J. 2010 Nov 17;99(10):L84-6. doi: 10.1016/j.bpj.2010.09.015.

Abstract

Zinc-induced aggregation of amyloid-β peptide (Aβ) is a hallmark molecular feature of Alzheimer's disease. Here we provide direct thermodynamic evidence that elucidates the role of the Aβ region 6-14 as the minimal Zn(2+) binding site wherein the ion is coordinated by His(6), Glu(11), His(13), and His(14). With the help of isothermal titration calorimetry and quantum mechanics/molecular mechanics simulations, the region 11-14 was determined as the primary zinc recognition site and considered an important drug-target candidate to prevent Zn(2+)-induced aggregation of Aβ.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Peptides / chemistry
  • Amyloid beta-Peptides / metabolism*
  • Binding Sites
  • Calorimetry
  • Computer Simulation
  • Mutant Proteins / metabolism
  • Quantum Theory
  • Thermodynamics
  • Zinc / metabolism*

Substances

  • Amyloid beta-Peptides
  • Mutant Proteins
  • Zinc