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Enhanced Colorimetric Immunoassay Accompanying with Enzyme Cascade Amplification Strategy for Ultrasensitive Detection of Low-Abundance Protein

机译:增强的比色免疫分析与酶级联扩增策略相结合的低丰度蛋白质的超灵敏检测

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摘要

Methods based on enzyme labels have been developed for colorimetric immunoassays, but most involve poor sensitivity and are unsuitable for routine use. Herein, we design an enhanced colorimetric immunoassay for prostate-specific antigen (PSA) coupling with an enzyme-cascade-amplification strategy (ECAS-CIA). In the presence of target PSA, the labeled alkaline phosphatase on secondary antibody catalyzes the formation of palladium nanostructures, which catalyze 3,3′,5,5′-tetramethylbenzidine-H2O2 system to produce the colored products, thus resulting in the signal cascade amplification. Results indicated that the ECAS-CIA presents good responses toward PSA, and allows detection of PSA at a concentration as low as 0.05 ng mL−1. Intra- and inter-assay coefficients of variation are below 9.5% and 10.7%, respectively. Additionally, the methodology is validated for analysis of clinical serum specimens with consistent results obtained by PSA ELISA kit. Importantly, the ECAS-CIA opens a new horizon for protein diagnostics and biosecurity.
机译:已经开发了基于酶标记的方法用于比色免疫分析,但是大多数方法灵敏度低且不适合常规使用。在本文中,我们设计了一种增强的比色免疫分析法,用于前列腺特异性抗原(PSA)与酶级联扩增策略(ECAS-CIA)的耦合。在目标PSA存在下,二抗上标记的碱性磷酸酶催化钯纳米结构的形成,从而催化3,3',5,5'-四甲基联苯胺-H2O2系统产生有色产物,从而导致信号级联放大。结果表明,ECAS-CIA对PSA表现出良好的响应,并允许以低至0.05 ng mL -1 的浓度检测PSA。批内和批间变异系数分别低于9.5%和10.7%。此外,该方法已通过PSA ELISA试剂盒的验证,可用于临床血清标本的分析。重要的是,ECAS-CIA为蛋白质诊断和生物安全性开辟了新视野。

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