首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >An enzyme-free surface plasmon resonance biosensor for real-time detecting microRNA based on allosteric effect of mismatched catalytic hairpin assembly
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An enzyme-free surface plasmon resonance biosensor for real-time detecting microRNA based on allosteric effect of mismatched catalytic hairpin assembly

机译:基于不匹配催化发夹装配的变构效应的无酶表面等离子体共振生物传感器,用于实时检测microRNA

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摘要

MicroRNAs (miRNAs) play significant regulatory roles in a variety of diseases and have been emerging as a group of promising biomarkers in cancer cells. Here, a novel and simple surface plasmon resonance (SPR) biosensor was developed for specific and highly sensitive detection of target miRNA employing the mismatched catalytic hairpin assembly (CHA) amplification coupling with programmable streptavidin aptamer (SA-aptamer). The presence of target miRNA triggered the allosteric effect of CHA amplification, which brought about the recycling of the target miRNA and produced large amounts of CHA products and activated SA-aptemers. Meanwhile, the plentiful CHA products could hybridize with the capture probes on the sensor chip, and the massive activated SA-aptamers could capture the streptavidin to achieve enhancement and output of the detection signal. Benefiting from the outstanding performance of the enzyme-free CHA amplification and non-label SPR biosensor, the established biosensor exhibited simplified process, high sensitivity and good selectivity. Under the optimal conditions, this designed strategy could detect target miRNA down to 1 pM with a dynamic range from 5 pM to 100 nM, and was successfully applied to the determination of target miRNA spiked into human total RNA samples. Thus, this SPR-based biosensor might become a potential alternative tool for miRNA detection in medical research and early clinical diagnosis. (C) 2015 Elsevier B.V. All rights reserved.
机译:微小RNA(miRNA)在多种疾病中起着重要的调节作用,并且已作为癌细胞中的一组有前途的生物标志物出现。在这里,开发了一种新颖且简单的表面等离振子共振(SPR)生物传感器,用于使用不匹配的催化发夹装配(CHA)扩增与可编程链霉亲和素适体(SA-aptamer)进行特异性和高灵敏度的靶miRNA检测。靶标miRNA的存在触发了CHA扩增的变构效应,从而导致靶标miRNA的循环利用,并产生了大量CHA产物和活化的SA适配体。同时,丰富的CHA产物可以与传感器芯片上的捕获探针杂交,而大量的活化SA适体可以捕获链霉亲和素以增强和输出检测信号。得益于无酶CHA扩增和非标记SPR生物传感器的出色性能,已建立的生物传感器具有简化的过程,高灵敏度和良好的选择性。在最佳条件下,该设计策略可以检测低至1 pM的靶标miRNA,动态范围从5 pM到100 nM,并成功地应用于测定掺入人总RNA样品中的靶标miRNA。因此,这种基于SPR的生物传感器可能会成为医学研究和早期临床诊断中miRNA检测的潜在替代工具。 (C)2015 Elsevier B.V.保留所有权利。

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