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首页> 外文期刊>Scientific reports. >Enhanced Colorimetric Immunoassay Accompanying with Enzyme Cascade Amplification Strategy for Ultrasensitive Detection of Low-Abundance Protein
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Enhanced Colorimetric Immunoassay Accompanying with Enzyme Cascade Amplification Strategy for Ultrasensitive Detection of Low-Abundance Protein

机译:随着酶级联扩增策略的增强比色免疫测定,用于低丰度蛋白的超细检测

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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:基于酶标记的方法已经为比色免疫测定制定,但大多数涉及较差的敏感性并且不适合常规使用。在此,我们设计了具有酶 - 级联扩增策略(ECAS-CIA)的前列腺特异性抗原(PSA)偶联的增强的比色免疫测定。在靶PSA的存在下,二次抗体上标记的碱性磷酸酶催化钯纳米结构的形成,其催化3,3',5,5'-四甲基苯胺-H 2 O 2 < /子>系统生产彩色产品,从而导致信号级联放大。结果表明,ECAS-CIA对PSA呈现良好的反应,并允许以低至0.05≤XUP>α1的浓度检测PSA。分析和测定间变异系数分别低于9.5%和10.7%。另外,该方法验证了临床血清样品的分析,具有由PSA ELISA试剂盒获得的一致结果。重要的是,ECAS-CIA为蛋白质诊断和生物安全开辟了新的地平线。

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