Metal-dependent alpha-helix formation promoted by the glycine-rich octapeptide region of prion protein

FEBS Lett. 1996 Nov 4;396(2-3):248-52. doi: 10.1016/0014-5793(96)01104-0.

Abstract

Prion diseases share a common feature in that the normal cellular prion protein (PrP(C)) converts to a protease-resistant isoform PrP(Sc). The alpha-helix-rich C-terminal half of PrP(C) is partly converted into beta-sheet in PrP(Sc). We have examined by Raman spectroscopy the structure of an octapeptide PHGGGWGQ that appears in the N-terminal region of PrP(C) and a longer peptide containing the octapeptide region. The peptides do not assume any regular structure without divalent metal ions, whereas Cu(II) binding to the HGGG segment induces formation of alpha-helical structure on the C-terminal side of the peptide chain. The N-terminal octapeptide of prion protein may be a novel structural motif that acts as a promoter of alpha-helix formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Copper / metabolism*
  • Glycine / analysis
  • Humans
  • Molecular Sequence Data
  • Peptide Fragments / chemistry*
  • Peptide Fragments / metabolism
  • PrPC Proteins / chemistry*
  • PrPC Proteins / metabolism
  • Protein Structure, Secondary*
  • Spectrum Analysis, Raman

Substances

  • Peptide Fragments
  • PrPC Proteins
  • Copper
  • Glycine