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首页> 外文期刊>Analytical chemistry >Hybridization Chain Reaction Amplification of MicroRNA Detection with a Tetrahedral DNA Nanostructure-Based Electrochemical Biosensor
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Hybridization Chain Reaction Amplification of MicroRNA Detection with a Tetrahedral DNA Nanostructure-Based Electrochemical Biosensor

机译:基于四面体DNA纳米结构的电化学生物传感器的microRNA检测的杂交链反应扩增。

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摘要

There remains a great challenge in the sensitive detection of microRNA because of the short length and low abundance of microRNAs in cells. Here, we have demonstrated an ultrasensitive detection platform for microRNA by combining the tetrahedral DNA nanostructure probes and hybridization chain reaction (HCR) amplification. The detection limits for DNA and microRNA are 100 aM and 10 aM (corresponding to 600 microRNAs in a 100 μL sample), respectively. Compared to the widely used supersandwich amplification, the detection limits are improved by 3 orders of magnitude. The uncontrolled surface immobilization and consumption of target molecules that limit the amplification efficiency of supersandwich are eliminated in our platform. Taking advantage of DNA nanotechnology, we employed three-dimensional tetrahedral DNA nanostructure as the scaffold to immobilize DNA recognition probes to increase the reactivity and accessibility, while DNA nanowire tentacles are used for efficient signal amplification by capturing multiple catalytic enzymes in a highly ordered way. The synergetic effect of DNA tetrahedron and nanowire tentacles have proven to greatly improve sensitivity for both DNA and microRNA detection.
机译:由于microRNA的长度短且丰度低,因此在microRNA的灵敏检测中仍然存在很大的挑战。在这里,我们通过结合四面体DNA纳米结构探针和杂交链反应(HCR)扩增,证明了microRNA的超灵敏检测平台。 DNA和microRNA的检测限分别为100 aM和10 aM(对应于100μL样品中的600 microRNA)。与广泛使用的超夹心扩增相比,检测极限提高了3个数量级。在我们的平台上,消除了不受控制的表面固定化和目标分子的消耗,这些目标分子限制了超三明治的扩增效率。利用DNA纳米技术,我们采用三维四面体DNA纳米结构作为支架来固定DNA识别探针以提高反应性和可及性,而DNA纳米线触手则通过以高度有序的方式捕获多种催化酶来进行有效的信号放大。 DNA四面体和纳米线触手的协同作用已被证明可以大大提高DNA和microRNA检测的灵敏度。

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