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一种基于简单 G-四链体分子信标的生物传感器,用于高选择性检测 microRNA。

A simple G-quadruplex molecular beacon-based biosensor for highly selective detection of microRNA.

机构信息

College of Life and Environmental Sciences, Gannan Normal University, Ganzhou 341000, PR China; Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering, PR China; State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082, PR China.

College of Life and Environmental Sciences, Gannan Normal University, Ganzhou 341000, PR China; Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering, PR China.

出版信息

Biosens Bioelectron. 2017 Jan 15;87:552-557. doi: 10.1016/j.bios.2016.07.060. Epub 2016 Jul 19.

Abstract

MicroRNAs (miRNAs) family members are usually different from each other in one-base variation. The high sequence homology poses a challenge for miRNA analysis with single-base selectivity. On the basis of G-quadruplex molecular beacons (G4MB) and duplex-specific nuclease (DSN), we developed a simple and highly selective amplification biosensor for miRNA detection. G4MB with a G4 motif stem is used as recognition probe. In the present of target miRNAs, G4MB hybridizes with target miRNA perfectly and forms a G4MB-miRNA duplex. Then, DSN subsequently cleaves the G4MB of the G4MB-miRNA duplex to recycle the target miRNA, which leads to fluorescence signal amplification. In the absence of target miRNAs, DSN can not digest the stem of G4MB because of the protection of G4 motif, which eliminates the false positive signal, and produces low fluorescence background. Importantly, the powerful discriminating abilities of both G4MB and DSN make the novel sensor suitable for miRNAs detection with high single-base selectivity. Comparing with traditional linear ssDNA probe-DSN-based method, the signal response of similar miRNA sequences with one-base difference has been reduced from 24% to 6% by using this G4MB-DSN-based method. Moreover, this simple sensor also exhibits a good applicability in cancer cell samples and a multiplex capability in one sample with different miRNA targets, making it a promising strategy for clinical diagnostics.

摘要

miRNAs(miRNA)家族成员通常在一个碱基的变异上彼此不同。高序列同源性给具有单碱基选择性的 miRNA 分析带来了挑战。在四链体分子信标(G4MB)和双链特异性核酸酶(DSN)的基础上,我们开发了一种简单且高度选择性的 miRNA 检测放大生物传感器。具有 G4 基序茎的 G4MB 用作识别探针。在靶 miRNA 的存在下,G4MB 与靶 miRNA 完全杂交并形成 G4MB-miRNA 双链。然后,DSN 随后切割 G4MB-miRNA 双链中的 G4MB 以回收靶 miRNA,从而导致荧光信号放大。在没有靶 miRNA 的情况下,由于 G4 基序的保护,DSN 不能消化 G4MB 的茎,从而消除了假阳性信号,并产生低荧光背景。重要的是,G4MB 和 DSN 的强大区分能力使新型传感器适用于具有高单碱基选择性的 miRNA 检测。与传统的线性 ssDNA 探针-DSN 方法相比,使用这种 G4MB-DSN 方法,具有一个碱基差异的类似 miRNA 序列的信号响应已从 24%降低到 6%。此外,该简单传感器在癌细胞样本中也表现出良好的适用性,并在一个样本中具有不同的 miRNA 靶标,具有多重能力,使其成为临床诊断的有前途的策略。

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