The distinct structural preferences of tau protein repeat domains

Chem Commun (Camb). 2018 May 31;54(45):5700-5703. doi: 10.1039/c8cc01263f.

Abstract

The tau fibrillar structures from the brain of an Alzheimer's patient have a core with a C-shaped motif of the third and fourth repeat domains (R3-R4). Our simulations indicated that the C-shaped motif is only stable for R3-R4, while R1-R2 tends to be linear in shape. These two structural motifs appear in the most stable K18 protofilament. Heparin can further stabilize the C-shaped R3-R4 motif, but not other repeats.

MeSH terms

  • Heparin / chemistry*
  • Humans
  • Hydrogen Bonding
  • Molecular Dynamics Simulation
  • Protein Aggregates
  • Protein Binding
  • Protein Domains
  • Protein Multimerization
  • Protein Stability
  • Protein Structure, Secondary
  • Repetitive Sequences, Amino Acid
  • tau Proteins / chemistry*

Substances

  • Protein Aggregates
  • tau Proteins
  • Heparin