Ontology highlight
ABSTRACT:
SUBMITTER: Marin-Moreno A
PROVIDER: S-EPMC6684573 | biostudies-literature | 2019 Aug
REPOSITORIES: biostudies-literature
Marín-Moreno Alba A Aguilar-Calvo Patricia P Moudjou Mohammed M Espinosa Juan Carlos JC Béringue Vincent V Torres Juan María JM
Scientific reports 20190806 1
Prion diseases are caused by the conversion of physiological PrP<sup>C</sup> into the pathogenic misfolded protein PrP<sup>Sc</sup>, conferring new properties to PrP<sup>Sc</sup> that vary upon prion strains. In this work, we analyze the thermostability of three prion strains (BSE, RML and 22L) that were heated at 98 °C for 2 hours. PrP<sup>Sc</sup> resistance to proteinase K (PrP<sup>res</sup>), residual infectivity by mouse bioassay and in vitro templating activity by protein misfolding cyclic ...[more]