Catalytic hairpin assembly induced dual signal enhancement for rapid detection of miRNA using fluorescence light-up silver nanocluster

被引:23
作者
Li, Ying [1 ]
Yu, Chuanfeng [1 ]
Zhao, Caisheng [1 ]
Ren, Chunnian [2 ]
Zhang, Xiaoru [1 ]
机构
[1] Qingdao Univ Sci & Technol, Key Lab Opt Elect Sensing & Analyt Chem Life Sci, State Key Lab Base Ecochem Engn,Shandong Key Lab, Key Lab Analyt Chem Life Sci Univ Shandong,Coll C, Qingdao 266042, Shandong, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Informat Sci & Technol, Qingdao 266042, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Catalytic hairpin assembly; Dual signal enhancement; Fluorescence light-up silver nanoduster; miRNA; MICRORNAS; EXPRESSION; BIOSENSOR; SENSOR; ASSAY;
D O I
10.1016/j.aca.2019.08.007
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel method of catalytic hairpin assembly (CHA) induced dual signal enhancement is developed for rapid detection of miRNA based on fluorescence light-up silver nanocluster (Ag NC). By the hybridization of a hairpin DNA and a single-stranded DNA, a unique probe is firstly designed. In the terminals of this probe, DNA-Ag NCs can be formed and display very weak fluorescence. In the presence of the target miRNA, the reaction of CHA can be triggered, forming two kinds of double-stranded complexes, in which the terminal DNA-Ag NCs are in close proximity to G-rich overhangs and the fluorescent signal can be dramatically enhanced. Compared with many other enzyme-based amplification strategies, this one exhibits distinct advantages of simplicity in experimental operation and a rapid detection process (within 1 h). Moreover, this assay exhibits an excellent selectivity and is successfully applied in the detection of miRNAs in complex biological media, which confirms the reliability and practicality of this protocol. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:93 / 98
页数:6
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