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发夹适体结构的靶标诱导转换用于通过外切酶催化的靶标循环扩增进行无标记和灵敏的荧光检测 ATP。

Target-induced structure switching of hairpin aptamers for label-free and sensitive fluorescent detection of ATP via exonuclease-catalyzed target recycling amplification.

机构信息

Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

Biosens Bioelectron. 2014 Jan 15;51:293-6. doi: 10.1016/j.bios.2013.08.002. Epub 2013 Aug 9.

DOI:10.1016/j.bios.2013.08.002
PMID:23974161
Abstract

In this work, we described the development of a new label-free, simple and sensitive fluorescent ATP sensing platform based on exonuclease III (Exo III)-catalyzed target recycling (ECTR) amplification and SYBR Green I indicator. The hairpin aptamer probes underwent conformational structure switching and re-configuration in the presence of ATP, which led to catalytic cleavage of the re-configured aptamers by Exo III to release ATP and to initiate the ECTR process. Such ECTR process resulted in the digestion of a significant number of the hairpin aptamer probes, leading to much less intercalation of SYBR Green I to the hairpin stems and drastic suppression of the fluorescence emission for sensitive ATP detection down to the low nanomolar level. Due to the highly specific affinity bindings between aptamers and ATP, the developed method exhibited excellent selectivity toward ATP against other analogous molecules. Besides, our ATP sensing approach used un-modified aptamer probes and could be performed in a "mix-and-detect" fashion in homogenous solutions. All these distinct advantages of the developed method thus made it hold great potential for the development of simple and robust sensing strategies for the detection of other small molecules.

摘要

在这项工作中,我们描述了一种新的无标记、简单和灵敏的荧光 ATP 传感平台的开发,该平台基于外切酶 III(Exo III)-催化的目标循环(ECTR)扩增和 SYBR Green I 指示剂。发夹适体探针在存在 ATP 的情况下经历构象结构切换和重新配置,这导致经重新配置的适体被 Exo III 催化切割以释放 ATP,并启动 ECTR 过程。这种 ECTR 过程导致大量的发夹适体探针被消化,导致 SYBR Green I 更少地嵌入发夹茎中,并且荧光发射被强烈抑制,从而能够灵敏地检测低纳摩尔级别的 ATP。由于适体和 ATP 之间具有高度特异性的亲和力结合,因此所开发的方法对 ATP 具有优异的选择性,而对其他类似分子则没有。此外,我们的 ATP 传感方法使用未经修饰的适体探针,并可以在均相溶液中以“混合和检测”的方式进行。因此,该方法的所有这些独特优势使其在开发用于检测其他小分子的简单而稳健的传感策略方面具有巨大潜力。

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