Seeded conversion of recombinant prion protein to a disulfide-bonded oligomer by a reduction-oxidation process

• DOI: 10.1038/nsb961
• Publication Date: 2003-08-05T16:50:40Z
• Authors: Sangho Lee; David Eisenberg
• Keywords: Models, Molecular; 0303 health sciences; Prions; Immunoblotting; Hydrogen-Ion Concentration; Recombinant Proteins; Protein Structure, Tertiary; Microscopy, Electron; 03 medical and health sciences; X-Ray Diffraction; Cricetinae; Animals; Electrophoresis, Polyacrylamide Gel; Disulfides; Endopeptidase K; Oxidation-Reduction; Plasmids; Protein Binding

The infectious form of prion protein, PrP(Sc), self-propagates by its conversion of the normal, cellular prion protein molecule PrP(C) to another PrP(Sc) molecule. It has not yet been demonstrated that recombinant prion protein can convert prion protein molecules from PrP(C) to PrP(Sc). Here we show that recombinant hamster prion protein is converted to a second form, PrP(RDX), by a redox process in vitro and that this PrP(RDX) form seeds the conversion of other PrP(C) molecules to the PrP(RDX) form. The converted form shows properties of oligomerization and seeded conversion that are characteristic of PrP(Sc). We also find that the oligomerization can be reversed in vitro. X-ray fiber diffraction suggests an amyloid-like structure for the oligomerized prion protein. A domain-swapping model involving intermolecular disulfide bonds can account for the stability and coexistence of two molecular forms of prion protein and the capacity of the second form for self-propagation.