Predicting the location of the non-local contacts in α-synuclein

Biochim Biophys Acta Proteins Proteom. 2018 Dec;1866(12):1201-1208. doi: 10.1016/j.bbapap.2018.09.006. Epub 2018 Sep 29.

Abstract

In this paper, the Sequential Collapse Model (SCM) for protein folding pathways is applied to investigate the location of the non-local contacts in the intrinsically disordered state of α-synuclein, a protein implicated in the onset and spreading of several serious neurodegenerative diseases. The model relies on the entropic cost of forming protein loops due to self-crowding effects, and the protein sequence to determine contact location and stability. It is found that the model predicts the existence of several possible non-local contacts, and the location of the non-local contacts is consistent with existing experimental evidence. The bearing of these findings on the pathogenic mechanism and its regulation is discussed.

Keywords: Disordered proteins; Neurodegeneration; Non-local contacts; Parkinson; Protein dynamics; Synuclein.

MeSH terms

  • Amino Acid Sequence
  • Entropy
  • Humans
  • Models, Molecular*
  • Mutagenesis, Site-Directed
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / pathology
  • Protein Folding
  • Protein Stability
  • alpha-Synuclein / chemistry
  • alpha-Synuclein / genetics
  • alpha-Synuclein / metabolism*

Substances

  • alpha-Synuclein