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首页> 外文期刊>Chemistry: A European journal >Label-free detection of microRNA: Two-step signal enhancement with a hairpin-probe-based graphene fluorescence switch and isothermal amplification
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Label-free detection of microRNA: Two-step signal enhancement with a hairpin-probe-based graphene fluorescence switch and isothermal amplification

机译:microRNA的无标记检测:基于基于发夹探针的石墨烯荧光开关和等温扩增的两步信号增强

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摘要

A label-free approach with multiple enhancement of the signal for microRNA detection has been introduced. The key idea of this strategy is achieved by taking advantage of a novel graphene oxide (GO)/intercalating dye based fluorescent hairpin probe (HP) and an isothermal polymerization reaction. In this paper, we used microRNA-21 (mir-21) as the target to examine the desirable properties of this assay. When the target, as a "trigger", was hybridized with the HP and caused a conformation change, an efficient isothermal polymerization reaction was activated to achieve the first step of the "signal" amplification. After incubation with the platform of GO/intercalating dye, the formed complex of DNA interacted with the high-affinity dye and then detached from the surface of the GO, a process that was accompanied by distinguishable fluorescence recovery. Further signal enhancement has been accomplished by a mass of intercalating dye inserting into the minor groove of the long duplex replication product. Due to the efficient and multiple amplification steps, this approach exerted a substantial enhancement in sensitivity and could be used for rapid and selective detection of Mir-21 at attomole levels. Proof-of-concept evidence has been provided for the proposed cost-effective strategy; thus, this strategy could expand the application of GO-material-based bioanalysis for nucleic acid studies.
机译:已经引入了无标记方法,该方法具有多种信号增强作用,可用于microRNA检测。该策略的关键思想是通过利用新型的氧化石墨烯(GO)/基于嵌入染料的荧光发夹探针(HP)和等温聚合反应来实现的。在本文中,我们使用microRNA-21(mir-21)作为靶标来检查该测定法的理想特性。当作为“触发”的目标与HP杂交并引起构象变化时,有效的等温聚合反应被激活,以实现“信号”扩增的第一步。用GO /嵌入染料平台孵育后,形成的DNA络合物与高亲和力染料相互作用,然后从GO表面脱离,此过程伴随着明显的荧光恢复。通过大量插入染料插入长双链体复制产物的小沟中,可以实现进一步的信号增强。由于有效且多重的扩增步骤,该方法显着提高了灵敏度,可用于快速和选择性地检测attomole水平的Mir-21。已经为拟议的具有成本效益的战略提供了概念证明;因此,该策略可以扩展基于GO材料的生物分析在核酸研究中的应用。

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