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The central hallmark of prion diseases is the misfolding of cellular prion protein (PrPC) into a disease-associated aggregated isoform known as scrapie prion protein (PrPSc). NMR spectroscopy has made many essential contributions to the characterization of recombinant PrP in its folded, unfolded and aggregated states. Recent studies reporting on de novo generation of prions from recombinant PrP and...
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