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- W2104014778 abstract "Several lines of evidence suggest that the normal form of the prion protein, PrP(C), exerts a neuroprotective activity against cellular stress or toxicity. One of the clearest examples of such activity is the ability of wild-type PrP(C) to suppress the spontaneous neurodegenerative phenotype of transgenic mice expressing a deleted form of PrP (Δ32-134, called F35). To define domains of PrP involved in its neuroprotective activity, we have analyzed the ability of several deletion mutants of PrP (Δ23-31, Δ23-111, and Δ23-134) to rescue the phenotype of Tg(F35) mice. Surprisingly, all of these mutants displayed greatly diminished rescue activity, although Δ23-31 PrP partially suppressed neuronal loss when expressed at very high levels. Our results pinpoint the N-terminal, polybasic domain as a critical determinant of PrP(C) neuroprotective activity, and suggest that identification of molecules interacting with this region will provide important clues regarding the normal function of the protein. Small molecule ligands targeting this region may also represent useful therapeutic agents for treatment of prion diseases." @default.
- W2104014778 created "2016-06-24" @default.
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- W2104014778 date "2011-09-29" @default.
- W2104014778 modified "2023-10-14" @default.
- W2104014778 title "The N-Terminal, Polybasic Region Is Critical for Prion Protein Neuroprotective Activity" @default.
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- W2104014778 doi "https://doi.org/10.1371/journal.pone.0025675" @default.
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