<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Piro JR</submitter><funding>NIAID NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>e1002001</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3033378</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(2)</volume><pubmed_abstract>Single-stranded polyanions ≥40 bases in length facilitate the formation of hamster scrapie prions in vitro, and polyanions co-localize with PrP(Sc) aggregates in vivo. To test the hypothesis that intact polyanionic molecules might serve as a structural backbone essential for maintaining the infectious conformation(s) of PrP(Sc), we produced synthetic prions using a photocleavable, 100-base oligonucleotide (PC-oligo). In serial Protein Misfolding Cyclic Amplification (sPMCA) reactions using purified PrP(C) substrate, PC-oligo was incorporated into physical complexes with PrP(Sc) molecules that were resistant to benzonase digestion. Exposure of these nuclease-resistant prion complexes to long wave ultraviolet light (315 nm) induced degradation of PC-oligo into 5 base fragments. Light-induced</pubmed_abstract><journal>PLoS pathogens</journal><pubmed_title>In situ photodegradation of incorporated polyanion does not alter prion infectivity.</pubmed_title><pmcid>PMC3033378</pmcid><funding_grant_id>R01 NS046478</funding_grant_id><funding_grant_id>T32 AI007519</funding_grant_id><funding_grant_id>R01 NS055875</funding_grant_id><funding_grant_id>2R01 NS046478</funding_grant_id><pubmed_authors>Harris BT</pubmed_authors><pubmed_authors>Supattapone S</pubmed_authors><pubmed_authors>Piro JR</pubmed_authors></additional><is_claimable>false</is_claimable><name>In situ photodegradation of incorporated polyanion does not alter prion infectivity.</name><description>Single-stranded polyanions ≥40 bases in length facilitate the formation of hamster scrapie prions in vitro, and polyanions co-localize with PrP(Sc) aggregates in vivo. To test the hypothesis that intact polyanionic molecules might serve as a structural backbone essential for maintaining the infectious conformation(s) of PrP(Sc), we produced synthetic prions using a photocleavable, 100-base oligonucleotide (PC-oligo). In serial Protein Misfolding Cyclic Amplification (sPMCA) reactions using purified PrP(C) substrate, PC-oligo was incorporated into physical complexes with PrP(Sc) molecules that were resistant to benzonase digestion. Exposure of these nuclease-resistant prion complexes to long wave ultraviolet light (315 nm) induced degradation of PC-oligo into 5 base fragments. Light-induced</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Feb</publication><modification>2026-07-15T10:34:14.274Z</modification><creation>2026-07-03T03:12:19.863Z</creation></dates><accession>S-EPMC3033378</accession><cross_references><pubmed>21304885</pubmed><doi>10.1371/journal.ppat.1002001</doi></cross_references></HashMap>