The molecular basis of distinct aggregation pathways of islet amyloid polypeptide

J Biol Chem. 2011 Feb 25;286(8):6291-300. doi: 10.1074/jbc.M110.166678. Epub 2010 Dec 10.

Abstract

Abnormal aggregation of islet amyloid polypeptide (IAPP) into amyloid fibrils is a hallmark of type 2 diabetes. In this study, we investigated the initial oligomerization and subsequent addition of monomers to growing aggregates of human IAPP at the residue-specific level using NMR, atomic force microscopy, mass spectroscopy, and computational simulations. We found that in solution IAPPs rapidly associate into transient low-order oligomers such as dimers and trimers via interactions between histidine 18 and tyrosine 37. This initial event is proceeded by slow aggregation into higher-order spherical oligomers and elongated fibrils. In these two morphologically distinct types of aggregates IAPPs adopt structures with markedly different residual flexibility. Here we show that the anti-amyloidogenic compound resveratrol inhibits oligomerization and amyloid formation via binding to histidine 18, supporting the finding that this residue is crucial for on-pathway oligomer formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid / chemistry*
  • Amyloid / genetics
  • Amyloid / metabolism
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism
  • Humans
  • Islet Amyloid Polypeptide / chemistry*
  • Islet Amyloid Polypeptide / genetics
  • Islet Amyloid Polypeptide / metabolism
  • Microscopy, Atomic Force
  • Nuclear Magnetic Resonance, Biomolecular
  • Protein Multimerization*
  • Resveratrol
  • Stilbenes / chemistry

Substances

  • Amyloid
  • Islet Amyloid Polypeptide
  • Stilbenes
  • Resveratrol