Molecular model of prion transmission to humans

Michael Jones, D. Wight, R. Barron, M. Jeffrey, J. Manson, C. Prowse, J. W. Ironside, M. W. Head

Research output: Contribution to journalArticlepeer-review

Abstract

To assess interspecies barriers to transmission of transmissible spongiform encephalopathies (TSEs), we investigated the ability of disease-associated prion proteins (PrPd) to initiate conversion of the human normal cellular form of prion protein of the 3 major PRNP polymorphic variants in vitro. Protein misfolding cyclic amplification showed that conformation of PrPd partly determines host susceptibility.
Original languageEnglish
Pages (from-to)2013-6
Number of pages4
JournalEmerging Infectious Diseases
Volume15
Issue number12
DOIs
Publication statusPublished - Dec 2009

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