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Amyloid fibrils from the N-terminal prion protein fragment are infectious
Recombinant C-terminally truncated prion protein PrP23-144 (which corresponds to the Y145Stop PrP variant associated with a Gerstmann–Sträussler–Scheinker-like prion disease) spontaneously forms amyloid fibrils with a parallel in-register β-sheet architecture and β-sheet core mapping to residues ∼11...
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| Format: | Article |
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| Langue: | en |
| Publié: |
National Academy of Sciences
2016
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| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5137684/ https://ncbi.nlm.nih.gov/pubmed/27849581 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1610716113 |
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