Alpha-Synuclein Disease Mutations Are Structurally Defective and Locally Affect Membrane Binding

J Am Chem Soc. 2017 Mar 29;139(12):4254-4257. doi: 10.1021/jacs.6b05335. Epub 2017 Mar 20.

Abstract

The intrinsically disordered human protein alpha-Synuclein (αS) has a prominent role in Parkinson's disease (PD) pathology. Several familial variants of αS are correlated with inherited PD. Disease mutations have been shown to have an impact on lipid membrane binding. Here, using electron paramagnetic resonance spectroscopy in combination with site-directed spin labeling, we show that familial PD-associated variants are structurally defective in membrane binding and alter the local binding properties of the protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Electron Spin Resonance Spectroscopy
  • Humans
  • Lipid Bilayers / metabolism*
  • Mutation
  • Parkinson Disease / genetics*
  • Parkinson Disease / metabolism
  • alpha-Synuclein / genetics*
  • alpha-Synuclein / metabolism

Substances

  • Lipid Bilayers
  • SNCA protein, human
  • alpha-Synuclein