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A 'turn-on' fluorescent copper biosensor based on DNA cleavage-dependent graphene-quenched DNAzyme

机译:基于DNA裂解依赖性石墨烯猝灭的DNA酶的“开启”荧光铜生物传感器

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摘要

A novel and promising "turn-on" fluorescent Cu~(2+) biosensor is designed based on graphene-DNAzyme catalytic beacon. Due to the essential surface and quenching properties of two-dimensional graphene, it can function as both "scaffold" and "quencher" of the Cu~(2+)-dependent DNAzyme, facilitating the formation of self-assembled graphene-quenched DNAzyme complex. However, Cu~(2+)-induced catalytic reaction disturbs the graphene-DNAzyme conformation, which will produce internal DNA cleavage-dependent effect. In this case, the quenched fluorescence in graphene-DNAzyme is quickly recovered to a large extent in 15min. Compared with common DNAzyme-based sensors, the presented graphene-based catalytic beacon greatly improves the signal-to-background ratio, hence increasing the sensitivity (LOD=0.365nM). Furthermore, the controllable DNA cleavage reaction provides an original and alternative internal method to regulate the interaction between graphene and DNA relative to the previous external sequence-specific hybridization-dependent regulation, which will open new opportunities for nucleic studies and sensing applications in the future.
机译:基于石墨烯-DNAzyme催化信标设计了一种新颖而有前途的“开通”荧光Cu〜(2+)生物传感器。由于二维石墨烯的基本表面和淬灭特性,它既可以充当依赖Cu〜(2+)的DNAzyme的“支架”又可以充当“猝灭剂”,从而促进自组装石墨烯猝灭的DNAzyme复合物的形成。 。然而,Cu〜(2+)诱导的催化反应扰乱了石墨烯-DNAzyme的构象,这将产生内部DNA裂解依赖性效应。在这种情况下,石墨烯-DNAzyme中淬灭的荧光会在15分钟内迅速恢复到很大程度。与普通的基于DNAzyme的传感器相比,本文提出的基于石墨烯的催化信标极大地提高了信噪比,从而提高了灵敏度(LOD = 0.365nM)。此外,相对于以前的外部序列特异性杂交依赖性调节,可控的DNA裂解反应提供了一种原始的和替代的内部方法来调节石墨烯和DNA之间的相互作用,这将为未来的核酸研究和传感应用打开新的机会。

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