Locally disordered conformer of the hamster prion protein: a crucial intermediate to PrPSc?

Biochemistry. 2002 Oct 15;41(41):12277-83. doi: 10.1021/bi026129y.

Abstract

A crucial step for transformation of the normal cellular isoform of the prion protein (PrP(C)) to the infectious prion protein (PrP(Sc)) is thought to entail a previously uncharacterized intermediate conformer, PrP*, which interacts with a template PrP(Sc) molecule in the conversion process. By carrying out (15)N-(1)H two-dimensional NMR measurements under variable pressure on Syrian hamster prion protein rPrP(90-231), we found a metastable conformer of PrP(C) coexisting at a population of approximately 1% at pH 5.2 and 30 degrees C, in which helices B and C are preferentially disordered. While the identity is still unproven, this observed metastable conformer is most logically PrP* or a closely related precursor. The structural characteristics of this metastable conformer are consistent with available immunological and pathological information about the prion protein.

Publication types

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

MeSH terms

  • Animals
  • Cold Temperature
  • Cricetinae
  • Mesocricetus
  • Nitrogen Isotopes
  • Nuclear Magnetic Resonance, Biomolecular
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • PrPSc Proteins / chemistry*
  • PrPSc Proteins / metabolism*
  • Pressure
  • Protein Conformation
  • Protein Folding
  • Protein Structure, Secondary
  • Protons
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Thermodynamics

Substances

  • Nitrogen Isotopes
  • Peptide Fragments
  • PrPSc Proteins
  • Protons
  • Recombinant Proteins