The formation of a novel supramolecular structure by amyloid of poly-L-glutamic acid

Biochem Biophys Res Commun. 2008 May 9;369(3):830-4. doi: 10.1016/j.bbrc.2008.02.085. Epub 2008 Feb 26.

Abstract

Polyglutamic acid (PE) has been shown to form amyloid fibrils in vitro under pH value of 4.0. However, under the pH of 2.0, a further self-association process resulting in a novel supramolecular structure was observed. These supramolecular assemblies had diameters ranging from 1 to 20 microm and lengths up to several hundred microns, which were significantly larger than those of typical "amyloid fibrils". The existence of amyloid-like structure within these assemblies was confirmed with Fourier transform infrared spectroscopy and Thioflavin T fluorescence assay. The aggregation process of PE was studied by direct observation of electronic microscopy. The supramolecular assemblies appeared to be formed in a hierarchical process in which the preformed amyloid-like subunits self-assembled into higher-order assemblies in a well-organized pattern.

MeSH terms

  • Amyloid / chemistry*
  • Amyloid / ultrastructure*
  • Benzothiazoles
  • Fluorescent Dyes / chemistry
  • Hydrogen-Ion Concentration
  • Kinetics
  • Microscopy, Electron, Scanning
  • Molecular Structure
  • Polyglutamic Acid / chemistry*
  • Spectroscopy, Fourier Transform Infrared
  • Thiazoles / chemistry

Substances

  • Amyloid
  • Benzothiazoles
  • Fluorescent Dyes
  • Thiazoles
  • thioflavin T
  • Polyglutamic Acid