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• W1982802234 endingPage "2848" @default.
• W1982802234 startingPage "2841" @default.
• W1982802234 abstract "Abnormal forms of prion protein (PrPSc) accumulate via structural conversion of normal PrP (PrPC) in the progression of transmissible spongiform encephalopathy. Under cell-free conditions, the process can be efficiently replicated using in vitro PrPSc amplification methods, including protein misfolding cyclic amplification. These methods enable ultrasensitive detection of PrPSc; however, there remain difficulties in utilizing them in practice. For example, to date, several rounds of protein misfolding cyclic amplification have been necessary to reach maximal sensitivity, which not only take several weeks, but also result in an increased risk of contamination. In this study, we sought to further promote the rate of PrPSc amplification in the protein misfolding cyclic amplification technique using mouse transmissible spongiform encephalopathy models infected with either mouse-adapted bovine spongiform encephalopathy or mouse-adapted scrapie, Chandler strain. Here, we demonstrate that appropriate regulation of sonication dramatically accelerates PrPSc amplification in both strains. In fact, we reached maximum sensitivity, allowing the ultrasensitive detection of < 1 LD50 of PrPSc in the diluted brain homogenates, after only one or two reaction rounds, and in addition, we detected PrPSc in the plasma of mouse-adapted bovine spongiform encephalopathy-infected mice. We believe that these results will advance the establishment of a fast, ultrasensitive diagnostic test for transmissible spongiform encephalopathies." @default.
• W1982802234 created "2016-06-24" @default.
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• W1982802234 date "2009-05-01" @default.
• W1982802234 modified "2023-10-16" @default.
• W1982802234 title "Hyperefficient PrP^Scamplification of mouse-adapted BSE and scrapie strain by protein misfolding cyclic amplification technique" @default.
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• W1982802234 doi "https://doi.org/10.1111/j.1742-4658.2009.07007.x" @default.
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