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NMR Structure of the Human Prion Protein with the Pathological Q212P Mutation Reveals Unique Structural Features

Prion diseases are fatal neurodegenerative disorders caused by an aberrant accumulation of the misfolded cellular prion protein (PrP(C)) conformer, denoted as infectious scrapie isoform or PrP(Sc). In inherited human prion diseases, mutations in the open reading frame of the PrP gene (PRNP) are hypo...

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Detalhes bibliográficos
Main Authors: Ilc, Gregor, Giachin, Gabriele, Jaremko, Mariusz, Jaremko, Łukasz, Benetti, Federico, Plavec, Janez, Zhukov, Igor, Legname, Giuseppe
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2908606/
https://ncbi.nlm.nih.gov/pubmed/20661422
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0011715
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