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Mammalian prion amyloid formation in bacteria

Mammalian prion proteins (PrPs) that cause transmissible spongiform encephalopathies are misfolded conformations of the host cellular PrP. The misfolded form, the scrapie PrP (PrP(Sc)), can aggregate into amyloid fibrils that progressively accumulate in the brain, evolving to a pathological phenotyp...

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Detalles Bibliográficos
Publicado en:Prion
Main Authors: Macedo, Bruno, Cordeiro, Yraima, Ventura, Salvador
Formato: Artigo
Idioma:Inglês
Publicado: Taylor & Francis 2016
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4981191/
https://ncbi.nlm.nih.gov/pubmed/26910379
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2016.1141859
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