Alpha Synuclein Fibrils Contain Multiple Binding Sites for Small Molecules

ACS Chem Neurosci. 2018 Nov 21;9(11):2521-2527. doi: 10.1021/acschemneuro.8b00177. Epub 2018 May 16.

Abstract

The fibrillary aggregation of the protein alpha synuclein (Asyn) is a hallmark of Parkinson's disease, and the identification of small molecule binding sites on fibrils is essential to the development of diagnostic imaging probes. A series of molecular modeling, photoaffinity labeling, mass spectrometry, and radioligand binding studies were conducted on Asyn fibrils. The results of these studies revealed the presence of three different binding sites within fibrillar Asyn capable of binding small molecules with moderate to high affinity. A knowledge of the amino acid residues in these binding sites will be important in the design of high affinity probes capable of imaging fibrillary species of Asyn.

Keywords: Alpha synuclein; Lewy bodies; Lewy neurites; Parkinson’s disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Binding Sites
  • Brain / diagnostic imaging
  • Brain / metabolism*
  • Humans
  • Mass Spectrometry
  • Molecular Docking Simulation
  • Molecular Dynamics Simulation
  • Parkinson Disease / diagnostic imaging
  • Parkinson Disease / metabolism*
  • Photoaffinity Labels
  • Positron-Emission Tomography
  • Protein Aggregates*
  • Protein Conformation, beta-Strand
  • Radioligand Assay
  • alpha-Synuclein / chemistry*
  • alpha-Synuclein / metabolism

Substances

  • Photoaffinity Labels
  • Protein Aggregates
  • alpha-Synuclein