Pharmacological chaperone for the structured domain of human prion protein

In prion diseases, the misfolded protein aggregates are derived from cellular prion protein (PrP(C)). Numerous ligands have been reported to bind to human PrP(C) (huPrP), but none to the structured region with the affinity required for a pharmacological chaperone. Using equilibrium dialysis, we scre...

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Autors principals: Nicoll, Andrew J., Trevitt, Clare R., Tattum, M. Howard, Risse, Emmanuel, Quarterman, Emma, Ibarra, Amaurys Avila, Wright, Connor, Jackson, Graham S., Sessions, Richard B., Farrow, Mark, Waltho, Jonathan P., Clarke, Anthony R., Collinge, John
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2010
Matèries:
Biological Sciences
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2955083/
https://ncbi.nlm.nih.gov/pubmed/20876144
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1009062107
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