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用于快速检测微小核糖核酸的双链置换生物传感器及无淬灭剂荧光策略

Double-Strand Displacement Biosensor and Quencher-Free Fluorescence Strategy for Rapid Detection of MicroRNA.

作者信息

Liao Rong, He Kui, Chen Chunyan, Chen Xiaoming, Cai Changqun

机构信息

Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University , Xiangtan, Hunan 411105, China.

出版信息

Anal Chem. 2016 Apr 19;88(8):4254-8. doi: 10.1021/acs.analchem.5b04154. Epub 2016 Apr 6.

Abstract

We describe a facile quencher-free fluorescence strategy for rapid detection of microRNAs (miRNAs) by using a novel double-strand displacement sensor. The sensor is designed with an outstanding 2-aminopurine (2-AP) fluorophore as a probe and a predesigned cDNA, which can completely complement the target miRNA and partly complement the 2-AP probe. When the target miRNA is added, the cDNA can be competed off from the cDNA\2-AP probe duplex, thereby forming a cDNA\RNA heteroduplex. The free 2-AP probe induces an increase in the fluorescent signal. A limit of detection of 5 nM and a wide linear range from 5 to 1000 nM (R(2) = 0.9971) are achieved by this assay. The rapid detection strategy can be accomplished within 2 h without expensive nanoparticles and complicated instruments for the whole procedure, thus, offering a significant potential for clinical application.

摘要

我们描述了一种简便的无淬灭剂荧光策略,用于通过使用新型双链置换传感器快速检测微小RNA(miRNA)。该传感器设计有出色的2-氨基嘌呤(2-AP)荧光团作为探针和预先设计的cDNA,其可以与靶miRNA完全互补并与2-AP探针部分互补。当加入靶miRNA时,cDNA可以从cDNA(2-AP探针双链体中被竞争掉,从而形成cDNA\RNA异源双链体。游离的2-AP探针导致荧光信号增加。该检测方法实现了5 nM的检测限和5至1000 nM的宽线性范围(R(2)=0.9971)。该快速检测策略可在2小时内完成,整个过程无需昂贵的纳米颗粒和复杂的仪器,因此在临床应用中具有巨大潜力。

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