Liao Rong, He Kui, Chen Chunyan, Chen Xiaoming, Cai Changqun
Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University , Xiangtan, Hunan 411105, China.
Anal Chem. 2016 Apr 19;88(8):4254-8. doi: 10.1021/acs.analchem.5b04154. Epub 2016 Apr 6.
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.
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。