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一种基于靶触发的双重扩增策略用于灵敏检测 microRNA。

A target-triggered dual amplification strategy for sensitive detection of microRNA.

机构信息

Department of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, Guangdong Province, PR China; Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Nanfang Hospital, Southern Medical University, Guangzhou 510515, Guangdong Province, PR China.

School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UK.

出版信息

Biosens Bioelectron. 2016 Sep 15;83:250-5. doi: 10.1016/j.bios.2016.04.053. Epub 2016 Apr 19.

Abstract

The accurate and quantitative analysis of microRNA (miRNA) expression is critical for biomedical research and clinical theranostics. In this study, we report a novel sensor for the sensitive detection of miRNA based on a duplex-specific nuclease (DSN)-assisted dual signal amplification strategy. A chimeric probe (DNA/2-OMe-RNA) that consists of a miRNA recognition DNA sequence and a Taqman probe hybridization RNA sequence (2'-O-methyl RNA) was designed and synthesized. One molecule of target miRNA can trigger cyclical cleavage of the chimeric probes to produce 2'-O-methyl RNA by DSN in the first round of amplification. The 2'-O-methyl RNA molecules can subsequently hybridize with Taqman probes and initiate the second round of cyclical amplification to generate detectable fluorescence by DSN. The proposed strategy exhibits high specificity in discriminating cognate miRNAs, and the dual signal transduction process enables the detection of miRNA concentrations as low as 7.3fM. We further applied this assay to miRNA quantification in cancer cells to confirm its applicability. The present study provides a sensitive, specific and simple method for miRNA detection and holds great potential for further application in biomedical research and in the clinical laboratory.

摘要

miRNA(微 RNA)表达的准确和定量分析对生物医学研究和临床治疗至关重要。在本研究中,我们报告了一种基于双链特异性核酸酶(DSN)辅助双重信号放大策略的 miRNA 敏感检测的新型传感器。设计并合成了一种嵌合探针(DNA/2-OMe-RNA),它由 miRNA 识别 DNA 序列和 Taqman 探针杂交 RNA 序列(2'-O-甲基 RNA)组成。目标 miRNA 的一个分子可以在第一轮扩增中通过 DSN 触发嵌合探针的循环切割,以产生 2'-O-甲基 RNA。随后,2'-O-甲基 RNA 分子可以与 Taqman 探针杂交,并通过 DSN 引发第二轮循环扩增,从而产生可检测的荧光。所提出的策略在区分同源 miRNA 时具有高特异性,并且双信号转导过程能够检测到低至 7.3fM 的 miRNA 浓度。我们进一步将该测定法应用于癌细胞中的 miRNA 定量,以证实其适用性。本研究为 miRNA 检测提供了一种灵敏、特异和简单的方法,在生物医学研究和临床实验室中有很大的应用潜力。

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