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Locally disordered conformer of the hamster prion protein: a crucial intermediate to PrPSc?
- Source :
-
Biochemistry [Biochemistry] 2002 Oct 15; Vol. 41 (41), pp. 12277-83. - Publication Year :
- 2002
-
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.
- Subjects :
- Animals
Cold Temperature
Cricetinae
Mesocricetus
Nitrogen Isotopes
Nuclear Magnetic Resonance, Biomolecular
Peptide Fragments chemistry
Peptide Fragments metabolism
Pressure
Protein Conformation
Protein Folding
Protein Structure, Secondary
Protons
Recombinant Proteins chemistry
Recombinant Proteins metabolism
Thermodynamics
PrPSc Proteins chemistry
PrPSc Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-2960
- Volume :
- 41
- Issue :
- 41
- Database :
- MEDLINE
- Journal :
- Biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12369815
- Full Text :
- https://doi.org/10.1021/bi026129y