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Toehold-mediated nonenzymatic amplification circuit on graphene oxide fluorescence switching platform for sensitive and homogeneous microRNA detection

机译:氧化石墨烯荧光切换平台上的脚趾介导的非酶放大电路,用于灵敏且均质的microRNA检测

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摘要

A novel graphene oxide (GO) fluorescence switch-based homogenous system has been developed to solve two problems that are commonly encountered in conventional GO-based biosensors. First, with the assistance of toehold-mediated nonenzymatic amplification (TMNA), the sensitivity of this system greatly surpasses that of previously described GO-based biosensors, which are always limited to the nM range due to the lack of efficient signal amplification. Second, without enzymatic participation in amplification, the unreliability of detection resulting from nonspecific desorption of DNA probes on the GO surface by enzymatic protein can be avoided. Moreover, the interaction mechanism of the double-stranded TMNA products contains several single-stranded toeholds at two ends and GO has also been explored with combinations of atomic force microscopy imaging, zeta potential detection, and fluorescence assays. It has been shown that the hybrids can be anchored to the surface of GO through the end with more unpaired bases, and that the other end, which has weaker interaction with GO, can escape GO adsorption due to the robustness of the central dsDNA structures. We verified this GO fluorescence switch-based detection system by detecting microRNA 21, an overexpressed non-encoding gene in a variety of malignant cells. Rational design of the probes allowed the isothermal nonenzymatic reaction to achieve more than 100-fold amplification efficiency. The detection results showed that our strategy has a detection limit of 10 pM and a detection range of four orders of magnitude. (C) 2015 Elsevier B.V. All rights reserved.
机译:已经开发了一种新颖的基于氧化石墨烯(GO)荧光开关的同质系统,以解决常规基于GO的生物传感器中经常遇到的两个问题。首先,在脚趾介导的非酶放大(TMNA)的辅助下,该系统的灵敏度大大超过了先前所述的基于GO的生物传感器,由于缺乏有效的信号放大,该传感器始终限于nM范围。第二,在没有酶参与扩增的情况下,可以避免由于酶蛋白在GO表面非特异性脱附DNA探针而导致检测的不可靠性。此外,双链TMNA产品的相互作用机理在两端包含多个单链脚尖,并且还通过结合原子力显微镜成像,ζ电位检测和荧光测定法探索了GO。已经显示,杂合体可以通过具有更多不成对碱基的末端锚定到GO的表面,并且与GO的相互作用较弱的另一末端由于中心dsDNA结构的坚固性而可以逃避GO吸附。我们通过检测microRNA 21(一种在多种恶性细胞中过度表达的非编码基因)验证了这种基于GO荧光开关的检测系统。探针的合理设计允许等温非酶反应达到100倍以上的扩增效率。检测结果表明,我们的策略的检测极限为10 pM,检测范围为四个数量级。 (C)2015 Elsevier B.V.保留所有权利。

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