首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >An enzyme free electrochemical biosensor for sensitive detection of miRNA with a high discrimination factor by coupling the strand displacement reaction and catalytic hairpin assembly recycling
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An enzyme free electrochemical biosensor for sensitive detection of miRNA with a high discrimination factor by coupling the strand displacement reaction and catalytic hairpin assembly recycling

机译:一种酶法电化学生物传感器,用于通过耦合链位移反应和催化发夹组装回收利用高辨别因子的miRNA敏感检测

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摘要

An isothermal, enzyme free, ultra-specific and ultra-sensitive protocol for electrochemical detection of miRNAs is proposed based on the toehold-mediated strand displacement reaction (SDR) and non-enzymatic catalytic hairpin reaction (CHA) recycling. The SDR was first triggered only in the presence of target miRNA and this process also affects other miRNA interferences having similar target sequences, thus guaranteeing a high discrimination factor and could be used in rare content miRNA detection with various amounts of interferences having similar target sequences. The output protector strand then triggered enzyme free CHA amplification and generates plenty of hairpin self-assembly products. This process in turn influences SDR equilibrium to move to the right and generates large amounts of protector output to ensure analysis sensitivity. Compared with traditional CHA, our proposed method greatly improved the signal to noise ratio and shows excellent performance in rare miRNA detection with miRNA analogue interference. Under the optimal experimental conditions and using square wave voltammetry, the established biosensor could detect target miRNA-21 down to 30 fM (S/N = 3) with a dynamic range from 100 fM to 2 nM, and discriminate rare target miRNA-21 from mismatched miRNA with high selectivity. This method holds great promise in miRNA detection from human cancer cell lines and would be a versatile and powerful tool for clinical molecular diagnostics.
机译:基于Toehold介导的链位移反应(SDR)和非酶促催化发夹反应(CHA)再循环,提出了用于MIRNA的电化学检测的等温,酶,超敏感方案。首先在靶miRNA存在下首先触发SDR,该方法还影响具有类似靶序列的其他miRNA干扰,从而保证高辨别因子,并且可以用具有类似靶序列的各种干扰的稀有含量miRNA检测。然后输出保护器链触发酶免疫扩增并产生大量发夹自组装产品。此过程反过来影响SDR平衡以向右移动,并产生大量的保护器输出,以确保分析灵敏度。与传统的CHA相比,我们所提出的方法大大改善了信噪比的信号,并在罕见的miRNA检测中显示出具有miRNA类似物干扰的优异性能。在最佳的实验条件下和使用方波伏安法,所建立的生物传感器可以检测目标miRNA-21至30 fm(s / n = 3),动态范围为100 fm至2nm,并辨别稀有目标miRNA-21具有高选择性的MiRNA不匹配。该方法在人类癌细胞系中的miRNA检测中具有很大的希望,并且是临床分子诊断的通用和强大的工具。

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