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Nanozyme-based bio-barcode assay for high sensitive and logic-controlled specific detection of multiple DNAs

机译:基于纳佐的生物条形码测定用于高敏感和逻辑控制的多个DNA的特异性检测

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摘要

Since HCV and HIV share a common transmission path, high sensitive detection of HIV and HCV gene is of significant importance to improve diagnosis accuracy and cure rate at early stage for HIV virus-infected patients. In our investigation, a novel nanozyme-based bio-barcode fluorescence amplified assay is successfully developed for simultaneous detection of HIV and HCV DNAs with excellent sensitivity in an enzyme-free and label-free condition. Here, bimetallic nanoparticles, PtAuNps, present outstanding peroxidase-like activity and act as barcode to catalyze oxidation of nonfluorescent substrate of amplex red (AR) into fluorescent resorufin generating stable and sensitive "Turn On" fluorescent output signal, which is for the first time to be integrated with bio-barcode strategy for fluorescence detection DNA. Furthermore, the provided strategy presents excellent specificity and can distinguish single-base mismatched mutant from target DNA. What interesting is that cascaded INHIBIT-OR logic gate is integrated with biosensors for the first time to distinguish individual target DNA from each other under logic function control, which presents great application in development of rapid and intelligent detection.
机译:由于HCV和HIV份额共同传播路径,因此HIV和HCV基因的高敏感性检测对于提高HIV病毒感染患者的早期诊断准确性和治愈率的显着性重视。在我们的研究中,成功​​开发了一种新型纳佐基的生物条形码荧光扩增测定,用于同时检测HIV和HCV DNA,在无酶和无标记条件下具有优异的敏感性。这里,PtaUnps,PtaUnps,具有卓越的过氧化物酶样活性,并作为条形码,以催化Amplex Red(Ar)的非荧光基材氧化成荧光超法产生稳定和敏感的“开启”荧光输出信号,这是第一次与生物条形码策略集成,用于荧光检测DNA。此外,提供的策略具有优异的特异性,并且可以将单碱基错配突变体与靶DNA区分开来。有趣的是,首次将级联抑制或逻辑门与生物传感器集成在一起,以在逻辑功能控制下彼此区分各个靶DNA,这在快速和智能检测的发展方面存在很大的应用。

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