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A sandwich-type electrochemical biosensing platform for microRNA-21 detection using carbon sphere-MoS_2 and catalyzed hairpin assembly for signal amplification

机译:夹心式电化学生物传感平台,用于使用碳球-MoS_2和催化发夹装配进行信号放大的microRNA-21检测

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In this work, a sandwich-type electrochemical biosensing platform is developed based on carbon sphere-MoS2 (CS-MoS2) and target recycling amplification of catalyzed hairpin assembly (CHA) strategy for ultrasensitive determination of microRNA (miRNA). The CS-MoS2 is prepared and used as sensing substrate, which shows high specific surface area, enhanced stability and good dispersibility. The capture probe is first modified on Au nanoparticles/CS-MoS2 modified glassy carbon electrode through Au-S band, and hairpin DNA1 (H1) then reacts with it and unfolds its loop domain by hybridizing with target miRNA-21. The opened H1 subsequently assembles with biotin labeled hairpin DNA 2 (H2) to displace the target. The liberated miRNA-21 is free and backs to the original solution to proceed next circulation, resulting in the generation of large amounts of H1-H2 duplex. Massive signal indicators horseradish peroxidase are then immobilized on electrode, and catalyze hydrogenperoxide + hydroquinone (H2O2 + HQ) system to produce a strong electrochemical response. The proposed assay benefits from advantages of sandwich-type structure, favorable electrochemical properties of CS-MoS2 and CHA target recycling amplification strategy. Therefore, it exhibits a wide linear relation between 1 x 10(-16) and 1 x 10(-10) M with a low detection limit of 1.6 x 10(-17) M for miRNA-21 detection.
机译:在这项工作中,开发了一种基于碳球-MoS2(CS-MoS2)的夹心型电化学生物传感平台,并针对超灵敏测定microRNA(miRNA)的催化发夹装配(CHA)策略进行靶标循环扩增。制备了CS-MoS2并用作传感基材,它具有高的比表面积,增强的稳定性和良好的分散性。首先通过Au-S带在Au纳米颗粒/ CS-MoS2修饰的玻碳电极上修饰捕获探针,然后发夹DNA1(H1)与之反应并通过与靶标miRNA-21杂交而展开其环域。随后,打开的H1与生物素标记的发夹DNA 2(H2)组装在一起,以置换目标。释放的miRNA-21是游离的,并返回原始溶液以进行下一个循环,从而导致生成大量的H1-H2双链体。然后将大量信号指示剂辣根过氧化物酶固定在电极上,并催化过氧化氢+对苯二酚(H2O2 + HQ)系统产生强烈的电化学响应。所提出的测定法得益于夹心型结构,CS-MoS2的良好电化学性能和CHA目标循环扩增策略的优势。因此,它在1 x 10(-16)和1 x 10(-10)M之间表现出宽的线性关系,而miRNA-21检测的检测限较低,只有1.6 x 10(-17)M。

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