Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments

Abstract

Despite their phenotypic heterogeneity, most human prion diseases belong to two broadly defined groups: Creutzfeldt-Jakob disease (CJD) and Gerstmann-Sträussler-Scheinker disease (GSS). While the structural characteristics of the disease-related proteinase K-resistant prion protein (resPrP ^D) associated with the CJD group are fairly well established, many features of GSS-associated resPrP ^D are unclear. Electrophoretic profiles of resPrP ^D associated with GSS variants typically show 6–8 kDa bands corresponding to the internal PrP fragments as well as a variable number of higher molecular weight bands, the molecular nature of which has not been investigated. Here we have performed systematic studies of purified resPrP ^D species extracted from GSS cases with the A117V (GSS ^A117V) and F198S (GSS ^F198S) PrP gene mutations. The combined analysis based on epitope mapping, deglycosylation treatment and direct amino acid sequencing by mass spectrometry provided a conclusive evidence that high molecular weight resPrP ^D species seen in electrophoretic profiles represent covalently-linked multimers of the internal ~ 7 and ~ 8 kDa fragments. This finding reveals a mechanism of resPrP ^D aggregate formation that has not been previously established in prion diseases.

Electronic supplementary material

The online version of this article (10.1186/s40478-019-0734-2) contains supplementary material, which is available to authorized users.