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 >Label-free and enzyme-free colorimetric detection of microRNA by catalyzed hairpin assembly coupled with hybridization chain reaction
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Label-free and enzyme-free colorimetric detection of microRNA by catalyzed hairpin assembly coupled with hybridization chain reaction

机译:催化发夹装配与杂交链反应相结合的无标记和无酶比色检测微小RNA

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摘要

In this study, a simple, label-free, and enzyme-free colorimetric biosensor has been developed for amplified detection of let-7a microRNA (miRNA) on the basis of dual signal amplification strategy. The sensing system mainly consists of four unlabeled hairpin probes termed H1, H2, H3, and H4. Upon sensing of the target miRNA, hairpin H1 is opened. Then hairpin H2 hybridizes with H1 forming H1-H2 duplex and frees the target miRNA that can be recycled to trigger another reaction cycle. In addition, the newly formed H1-H2 duplex hybridizes with hairpin H3, and this triggers the autonomous cross opening of the two hairpins H3 and H4 through hybridization chain reaction. During this process, numerous split G-quadruplex structures are generated and further associate with cofactor hemin to form massive peroxidase-mimicking DNAzymes. The resulting DNAzymes catalyze the H2O2-mediated oxidation of colorless 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS(2-)) to the green-colored ABTS(center dot-), inducing a remarkably amplified colorimetric signal. This newly developed sensing system exhibits high sensitivity toward miRNA with a detection limit of 7.4 fM and a large dynamic range of 6 orders of magnitude from 10 fM to 10 nM. Furthermore, it exhibits a good performance to discriminate single-base difference among the miRNA family members and holds a great potential for early diagnosis in gene-related diseases. (C) 2016 Elsevier B.V. All rights reserved.
机译:在这项研究中,基于双信号放大策略,已开发出一种简单,无标记和无酶的比色生物传感器,用于let-7a microRNA(miRNA)的扩增检测。传感系统主要由四个未标记的发夹探针组成,分别称为H1,H2,H3和H4。一旦检测到靶标miRNA,发夹H1就被打开。然后,发夹H2与H1杂交,形成H1-H2双链体,并释放靶标miRNA,可将其回收以触发另一个反应周期。另外,新形成的H1-H2双链体与发夹H3杂交,并且这通过杂交链反应触发两个发夹H3和H4的自主交叉开放。在这个过程中,产生了许多分裂的G-四链体结构,并进一步与辅因子血红素结合形成大量的过氧化物酶模拟DNA酶。产生的DNA酶催化H2O2介导的无色2,2'-叠氮基双(3-乙基苯并噻唑啉-6-磺酸)(ABTS(2-))氧化为绿色ABTS(中心点-)显着放大的比色信号。这种新开发的传感系统对miRNA具有高灵敏度,检测极限为7.4 fM,动态范围从10 fM到10 nM均为6个数量级。此外,它在区分miRNA家族成员之间的单碱基差异方面表现出良好的性能,并且在基因相关疾病的早期诊断方面具有巨大潜力。 (C)2016 Elsevier B.V.保留所有权利。

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