A simple electrochemical biosensor for highly sensitive and specific detection of microRNA based on mismatched catalytic hairpin assembly

被引:137
|
作者
Zhang, Ye [1 ]
Yan, Yurong [1 ]
Chen, Wenhong [2 ]
Cheng, Wei [3 ]
Li, Shengqiang [1 ]
Ding, Xiaojuan [1 ]
Li, Dandan [1 ]
Wang, Hong [1 ]
Ju, Huangxian [1 ,4 ]
Ding, Shijia [1 ]
机构
[1] Chongqing Med Univ, Key Lab Clin Lab Diagnost, Minist Educ, Coll Lab Med, Chongqing 400016, Peoples R China
[2] Chongqing Med Univ, Childrens Hosp, Dept Clin Lab, Chongqing 400014, Peoples R China
[3] Chongqing Med Univ, Affiliated Hosp 1, Ctr Clin Mol Med Detect, Chongqing 400016, Peoples R China
[4] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
MicroRNA; Catalytic hairpin assembly; Mismatched base pairs; Differential pulse voltammetry; Electrochemical biosensor; ROLLING CIRCLE AMPLIFICATION; ENZYME-FREE; ULTRASENSITIVE DETECTION; SIGNAL AMPLIFICATION; NONCODING RNA; CIRCUITS; STRATEGY; MIRNA; APTASENSOR; DESIGN;
D O I
10.1016/j.bios.2015.01.026
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
MicroRNAs (miRNAs) play vital regulatory roles in cancer development and a variety of diseases, which make them become promising biomarkers. Here, a simple electrochemical biosensor was developed for highly sensitive and specific detection of target miRNA using mismatched catalytic hairpin assembly (CHA). The target miRNA triggered the toehold strand displacement assembly of two hairpin substrates, which led to the cyclic reuse of the target miRNA and the CHA products. Compared with the traditional CHA, mismatched CHA could decrease the nonspecific CHA products, which reduced the background signal significantly. Under the optimal experimental conditions and using differential pulse voltammetry, the established biosensor could detect target miRNA down to 0.6 pM (S/N=3) with a linear range from 1 pM to 25 nM, and discriminate target miRNA from mismatched miRNA with a high selectivity. It was also applied to the determination of miRNA spiked into human total RNA samples. Thus, this biosensing strategy might become a potential alternative tool for detection of miRNA in biomedical research and early clinical diagnosis. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:343 / 349
页数:7
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