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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 >Target-triggered three-way junction in conjugation with catalytic concatemers-functionalized nanocomposites provides a highly sensitive colorimetric method for miR-21 detection
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Target-triggered three-way junction in conjugation with catalytic concatemers-functionalized nanocomposites provides a highly sensitive colorimetric method for miR-21 detection

机译:与催化联系人官能化纳米复合材料的缀合物的目标触发的三通交界处为miR-21检测提供了一种高敏感的比色方法

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摘要

With the great advances in DNA nanotechnology, scientists have shown interest in developing dynamic nanostructures for theranostic applications, analyte sensing and cargo delivery. Here, we present a specific enzyme free ultrasensitive platform based on a multilayer coupled signal amplification strategy to quantify miR-21 molecule. The biosensor was integrated based on three signal amplification gadgets, namely a translator mediated catalytic hairpin assembly (CHA), a multilayer DNA concatemer on the surface of gold decorated magnetic nanoparticle (GMNP), and a DNAzyme-mediated catalytic signal amplification. MiR-21 mediates the release of a DNA translator from an immobilized duplex to engage in a CHA reaction using three hairpins, including a GMNP-conjugated hairpin 1 (H1), biotin-labeled hairpin 2 (H2) and a GMNP-conjugated hairpin 3 (H3) to form a three-way junction (3WJ). Meanwhile, a plenty of initiator strand 0 (S0) on GMNPs - each of which has been bifunctionalized with S0/Hi or S0/H3 - drive several multilayer peroxidase-mimicking DNAzyme concatemers in the presence of two accessory oligonucleotides; strand 1 (Si) and strand 2 (S2). Since a G-rich sequence was attached at the 5'-end of S1 strand, in the presence of hemin cofactor, an active G-quadruplex DNAzyme with peroxidase activity was formed. The concatemers on the surface of GMNPs can convert a colorless substrate to a green product. The biosensor can detect as low as 1 aM of miR-21 and provide an excellent capability to discriminate single-base mismatches. The required time for the formulation of the assay reagents is about three days and the reaction time for the detection of miR-21 takes place in less than four hours.
机译:随着DNA纳米技术的巨大进展,科学家们已经表现出兴趣在为治疗系统,分析物传感和货物交付中发育动态纳米结构。这里,我们基于多层耦合信号放大策略介绍特定的酶自由致敏平台以定量miR-21分子。基于三个信号放大小工具集成了生物传感器,即翻译介导的催化发夹组件(CHA),金色装饰磁性纳米粒子(GMNP)表面上的多层DNA联系,以及DNazyme介导的催化信号扩增。 MiR-21介导DNA转换器的释放从固定的双链体中,使用三个发夹从生物蛋白,包括GMNP缀合的发夹1(H1),生物素标记的发夹2(H2)和GMNP-缀合的发夹3中的CHA反应(H3)形成三通交界处(3WJ)。同时,在GMNPS上的大量引发剂链0(S0) - 其中每一个与S0 / HI或S0 / H3分别化 - 在两种辅助寡核苷酸存在下驱动几种多层过氧化物酶模拟剂的二唑类化合物;链1(Si)和链2(S2)。由于在S1股的5'末端附着富含G的序列,因此在血红素辅因子的存在下,形成具有过氧化物酶活性的活性G- QuadflexDNazyme。 GMNPS表面上的联系人可以将无色衬底转换为绿色产品。生物传感器可以检测到miR-21的低至1μm,并提供优异的能力来区分单碱基错配。用于制剂的测定试剂的所需时间约为3天,并且在不到4小时的时间内进行检测的反应时间。

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