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Conserved amyloid core structure of stop mutants of the human prion protein

Prion diseases are associated with misfolding of the natively α-helical prion protein into isoforms that are rich in cross β-structure. However, both the mechanism by which pathological conformations are produced and their structural properties remain unclear. Using a combination of nuclear magnetic...

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Detalhes bibliográficos
Autor principal: Zweckstetter, Markus
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3783102/
https://ncbi.nlm.nih.gov/pubmed/23406905
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.23956
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