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Early Delivery of Misfolded PrP from ER to Lysosomes by Autophagy

Prion diseases are linked to the accumulation of a misfolded isoform (PrP(Sc)) of prion protein (PrP). Evidence suggests that lysosomes are degradation endpoints and sites of the accumulation of PrP(Sc). We questioned whether lysosomes participate in the early quality control of newly generated misf...

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Detalhes bibliográficos
Main Authors: Cortes, Constanza J., Qin, Kefeng, Norstrom, Eric M., Green, William N., Bindokas, Vytautas P., Mastrianni, James A.
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3877647/
https://ncbi.nlm.nih.gov/pubmed/24454378
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/560421
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