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Enhanced detection of prion infectivity from blood by preanalytical enrichment with peptoid-conjugated beads

机译:通过拟肽缀合的珠粒增强血液中血液中的朊病毒感染性的检测

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Prions cause transmissible infectious diseases in humans and animals and have been found to be transmissible by blood transfusion even in the presymptomatic stage. However, the concentration of prions in body fluids such as blood and urine is extremely low; therefore, direct diagnostic tests on such specimens often yield false-negative results. Quantitative preanalytical prion enrichment may significantly improve the sensitivity of prion assays by concentrating trace amounts of prions from large volumes of body fluids. Here, we show that beads conjugated to positively charged peptoids not only captured PrP aggregates from plasma of prion-infected hamsters, but also adsorbed prion infectivity in both the symptomatic and preclinical stages of the disease. Bead absorbed prion infectivity efficiently transmitted disease to transgenic indicator mice. We found that the readout of the peptoid-based misfolded protein assay (MPA) correlates closely with prion infectivity in vivo, thereby validating the MPA as a simple, quantitative, and sensitive surrogate indicator of the presence of prions. The reliable and sensitive detection of prions in plasma will enable a wide variety of applications in basic prion research and diagnostics.
机译:朊病毒导致人类和动物的传染病感染疾病,并且已经发现即使在假设阶段也被输血传播。然而,血液和尿液如血液和尿液中的朊病毒浓度极低;因此,对这种标本的直接诊断测试通常会产生假阴性结果。定量预级朊病毒富集可以通过从大量的体液中浓缩痕量的朊病毒来显着提高朊病毒测定的敏感性。在这里,我们表明,与带正电荷的肽的珠子共轭,不仅捕获了来自朊病毒的捕母等血浆的PRP聚集体,而且在疾病的症状和临床前阶段也吸附了朊病毒感染性。珠子吸收朊病毒感染有效地传播给转基因指示小鼠的疾病。我们发现,拟肽的错误折叠蛋白质测定(MPa)的读出与体内朊病毒感染性密切相关,从而将MPA验证为朊病毒存在的简单,定量和敏感的替代指标。等离子体中的可靠和敏感的朊病毒检测将在基础朊病毒研究和诊断中实现各种各样的应用。

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