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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| Publié dans: | Proc Natl Acad Sci U S A |
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| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
National Academy of Sciences
2001
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| Sujets: | |
| Accès en ligne: | 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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