Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Crystallographic Studies of Prion Protein (PrP) Segments Suggest How Structural Changes Encoded by Polymorphism at Residue 129 Modulate Susceptibility to Human Prion Disease

Journal Article · · J. Biol. Chem.
A single nucleotide polymorphism (SNP) in codon 129 of the human prion gene, leading to a change from methionine to valine at residue 129 of prion protein (PrP), has been shown to be a determinant in the susceptibility to prion disease. However, the molecular basis of this effect remains unexplained. In the current study, we determined crystal structures of prion segments having either Met or Val at residue 129. These 6-residue segments of PrP centered on residue 129 are 'steric zippers,' pairs of interacting {beta}-sheets. Both structures of these 'homozygous steric zippers' reveal direct intermolecular interactions between Met or Val in one sheet and the identical residue in the mating sheet. These two structures, plus a structure-based model of the heterozygous Met-Val steric zipper, suggest an explanation for the previously observed effects of this locus on prion disease susceptibility and progression.
Research Organization:
Advanced Photon Source (APS), Argonne National Laboratory (ANL), Argonne, IL (US)
Sponsoring Organization:
USDOE
OSTI ID:
1002728
Journal Information:
J. Biol. Chem., Journal Name: J. Biol. Chem. Journal Issue: 09, 2010 Vol. 285; ISSN JBCHA3; ISSN 0021-9258
Country of Publication:
United States
Language:
ENGLISH

Similar Records

Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): Codon 178 mutation and codon 129 polymorphism
Journal Article · Fri Oct 01 00:00:00 EDT 1993 · American Journal of Human Genetics; (United States) · OSTI ID:5052236

Conformational diversity in prion protein variants influences intermolecular [beta]-sheet formation
Journal Article · Mon Apr 19 00:00:00 EDT 2010 · EMBO J. · OSTI ID:1002277

Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD)
Journal Article · Thu Sep 30 20:00:00 EDT 1993 · American Journal of Human Genetics; (United States) · OSTI ID:5052442