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2000
Volume 12, Issue 3
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

The main hypothesis for prion diseases proposes that the cellular protein (PrPC) can be altered into a misfolded, β-sheet-rich isoform (PrPSc). We describe here that host nucleic acid may catalyze the conversion between PrPC and PrPSc isoforms, by reducing the protein mobility and by making the protein-protein interactions more likely. We summarize the findings, focusing in the biological relevance of the catalytic action of nucleic acid.

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/content/journals/ppl/10.2174/0929866053587138
2005-04-01
2025-05-23
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/content/journals/ppl/10.2174/0929866053587138
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  • Article Type:
    Review Article
Keyword(s): aggregation; catalysis; nucleic acid; prion; structural conversion
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