NR ALIN
AU Tagliavini,F.; Prelli,F.; Verga,L.; Giaccone,G.; Sarma,R.; Gorevic,P.; Ghetti,B.; Passerini,F.; Ghibaudi,E.; Forloni,G.; Salmona,M.; Bugiani,O.; Frangione,B.
TI Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro
QU Proceedings of the National Academy of Sciences of the United States of America 1993 Oct 15; 90(20): 9678-82
PT journal article
AB Gerstmann-Sträussler-Scheinker disease (GSS) is a prion-related encephalopathy pathologically characterized by massive deposition of prion protein (PrP) amyloid in the central nervous system. The major component of amyloid fibrils isolated from patients of the Indiana kindred of GSS (GSS-Ik) is an 11-kDa fragment of PrP spanning residues 58 to approximately 150. These patients carry a missense mutation of the PRNP gene, causing a Phe -> Ser substitution at codon 198. We investigated fibrillogenesis in vitro by using synthetic peptides homologous to consecutive segments of GSS-Ik amyloid protein (residues 57-64, 89-106, 106-126, and 127-147) as well as peptides from the PrP region with the GSS-Ik mutation (residues 191-205 and 181-205, both wild type and mutant). Peptide PrP-(106-126) formed straight fibrils similar to those extracted from GSS brains, whereas peptide PrP-(127-147) formed twisted fibrils resembling scrapie-associated fibrils isolated from subjects with transmissible spongiform encephalopathies. Congo red staining and x-ray fibril diffraction showed that both straight and twisted fibrils had tinctorial and conformational properties of native amyloid. Conversely, the other peptides did not form amyloid-like fibrils under similar conditions. These findings suggest that the sequence spanning residues 106-147 of PrP is central to amyloid fibril formation in GSS and related encephalopathies.
MH Amino Acid Sequence; Amyloid/*chemistry; Amyloid Neuropathies/pathology; Crystallography, X-Ray; Human; In Vitro; Microscopy, Electron; Molecular Sequence Data; Nerve Tissue Proteins/*chemistry; Peptides/chemistry; Polymers; PrPsc Proteins; Prions/*chemistry; Solubility; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S.
AD Istituto Nazionale Neurologico Carlo Besta, Milan, Italy.
SP englisch
PO USA