State Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410013, China.
Sensors (Basel). 2017 Apr 3;17(4):760. doi: 10.3390/s17040760.
MicroRNAs (miRNAs) act as biomarkers for the diagnosis of a variety of cancers. Since the currently used methods for miRNA detection have limitations, simple, sensitive, and cost-effective methods for the detection of miRNA are required. This work demonstrates a facile, quencher-free, fluorescence-based analytical method for cost-effective and sensitive detection of miRNA using a super 2-aminopurine (2-AP)-labeled hairpin probe (HP) and exonuclease I activity. Specifically, the fluorescence of 2-AP is strongly quenched when it is incorporated within DNA. In the presence of a target miRNA, HP attains an open conformation by hybridizing with the target miRNA to form a double-stranded structure with a protruding 3'-terminus. Next, the digestion of the protruding 3'-terminus is triggered by exonuclease I, during which 2-AP is released free in solution from the DNA, thereby increasing fluorescence. This method is highly sensitive, with a detection limit of 0.5 nM-10 times lower than a previously reported quencher-free fluorescence method. Furthermore, this method has potential applications in clinical diagnosis and biomedical research.
微 RNA(miRNA)可作为多种癌症诊断的生物标志物。由于目前 miRNA 检测方法存在局限性,因此需要简单、灵敏且具有成本效益的 miRNA 检测方法。本工作展示了一种基于超 2-氨基嘌呤(2-AP)标记发夹探针(HP)和核酸外切酶 I 活性的简便、无淬灭剂、基于荧光的分析方法,用于 miRNA 的经济高效和灵敏检测。具体而言,2-AP 掺入 DNA 内时其荧光会被强烈猝灭。在存在靶 miRNA 的情况下,HP 通过与靶 miRNA 杂交形成具有突出 3'-末端的双链结构而达到开环构象。接下来,核酸外切酶 I 触发突出 3'-末端的消化,在此过程中,2-AP 从 DNA 中游离释放到溶液中,从而增加荧光。该方法具有高度的灵敏度,检测限为 0.5 nM-10 倍低于先前报道的无淬灭剂荧光方法。此外,该方法在临床诊断和生物医学研究中具有潜在的应用。