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Journal ArticleDOI

Resistance of the scrapie agent to inactivation by psoralens.

TLDR
Five psoralens, at concentrations up to 500 times greater than those required to inactivate conventional viruses, did not influence scrapie agent titers in partially purified preparations from murine spleen and hamster brain.
Abstract
–In searching for a nucleic acid within the scrapie agent, we employed psoralens which penetrate the coats of most conventional viruses, form photoadducts with their genomes, and block replication of the viruses. Five psoralens, at concentrations up to 500 times greater than those required to inactivate conventional viruses, did not influence scrapie agent titers in partially purified preparations from murine spleen and hamster brain. 3H-psoralens were used to monitor the formation of photoadducts within nucleic acid standards added to preparations of the scrapie agent. Since no inhibition of psoralen photoadduct formation was observed in these preparations, one of three possibilities seems likely: the scrapie agent is devoid of nucleic acid, the psoralens failed to penetrate the protein coat of the agent, or its nucleic acid is unreactive with psoralens.

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Citations
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Journal ArticleDOI

Molecular biology of prion diseases

TL;DR: Understanding prion diseases may advance investigations of other neurodegenerative disorders and of the processes by which neurons differentiate, function for decades, and then grow senescent.
Journal ArticleDOI

Scrapie prion protein contains a phosphatidylinositol glycolipid

TL;DR: Observations indicate that PrPC is anchored to the cell surface by the glycolipid, which is derived from PrPSc by limited proteolysis at the amino terminus.
Journal ArticleDOI

Scrapie prions aggregate to form amyloid-like birefringent rods

TL;DR: The findings raise the possibility that the amyloid plaques observed in transmissible, degenerative neurological diseases might consist of prions, a polymeric form of the scrapie prion.
Journal ArticleDOI

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

TL;DR: The primary structure of PrP encoded by the gene of a healthy animal does not differ from that encoded by a cDNA from a scrapie-infected animal, suggesting that the different properties ofPrP from normal and scrapie -infected brains are due to post-translational events.
References
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Journal ArticleDOI

A simplification of the protein assay method of Lowry et al. which is more generally applicable

TL;DR: A simple method based on a linear log-log protein standard curve is presented to permit rapid and totally objective protein analysis using small programmable calculators.
Journal ArticleDOI

A Film Detection Method for Tritium‐Labelled Proteins and Nucleic Acids in Polyacrylamide Gels

TL;DR: A simple method for detecting 3H in polyacrylamide gels by scintillation autography (fluorography) using X-ray film, which is ten times more sensitive than conventional autoradiography of isotopes with higher emission energies.
Book ChapterDOI

[99] Determination of nucleic acids in tissues by pentose analysis

TL;DR: The extraction methods described were developed for nucleic acid determinations by spectrophotometric methods and it has become quite clear that the separations are not sufficiently refined for isotopic work.
Journal ArticleDOI

Chain length determination of small double- and single-stranded DNA molecules by polyacrylamide gel electrophoresis

TL;DR: The use of polyacrylamide gel electrophoresis to estimate chain lengths of double- and single-stranded DNA molecules in the size range 20-1000 base pairs (or nucleotides) is described.
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