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The crystal structure of an octapeptide repeat of the Prion protein in complex with a Fab fragment of the POM2 antibody
Prion diseases are progressive, infectious neurodegenerative disorders caused primarily by the misfolding of the cellular prion protein (PrP(c)) into an insoluble, protease-resistant, aggregated isoform termed PrP(sc). In native conditions, PrP(c) has a structured C-terminal domain and a highly flex...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Ltd
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3719084/ https://ncbi.nlm.nih.gov/pubmed/23629842 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pro.2270 |
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