A role for intermolecular disulfide bonds in prion diseases?

The key event in prion diseases seems to be the conversion of the prion protein PrP from its normal cellular isoform (PrP(C)) to an aberrant “scrapie” isoform (PrP(Sc)). Earlier studies have detected no covalent modification in the scrapie isoform and have concluded that the PrP(C) → PrP(Sc) convers...

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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Welker, Ervin, Wedemeyer, William J., Scheraga, Harold A.
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 2001
Soggetti:	Biological Sciences
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC31835/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11274354/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.071066598
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