Signal amplification detection of DNA using a sensor fabricated by one-step covalent immobilization of amino-terminated probe DNA onto the polydopamine-modified screen-printed carbon electrode

被引:42
作者
Zhang, Yonghua [1 ,2 ]
Geng, Xiaohui [1 ]
Ai, Junjie [1 ]
Gao, Qiang [1 ]
Qi, Honglan [1 ]
Zhang, Chengxiao [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Appl Surface & Colloid Chem, Xian 710062, Peoples R China
[2] Luoyang Normal Univ, Sch Chem & Chem Engineer, Luoyang 471022, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA sensor; Polydopamine; Screen-printed carbon electrode; AuNPs; Signal amplification; ELECTROCHEMICAL DETECTION; GOLD NANOPARTICLES; THIN-FILMS; GENOSENSOR; BIOSENSORS; NANOTUBES; DOPAMINE; IMMUNOSENSOR; IMPEDANCE;
D O I
10.1016/j.snb.2015.08.005
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An electrochemical DNA sensor was fabricated based on covalent immobilization of amino-terminated probe DNA onto the polydopamine (PDA) modified screen-printed carbon electrode (SPCE). Immobilization was achieved via one-step Schiff base reaction between the amino group of the probe DNA and quinones in PDA. FDA was formed via electrochemical polymerization of dopamine monomer on the SPCE surface. After a sandwich-type hybridization reaction, the gold nanoparticle-labeled reporter DNA was bound onto the DNA sensor surface to further induce silver deposition in the presence of silver enhancer solutions. The electrochemical stripping signal of the deposited silver nanoparticles in KCl solution was used to monitor the hybridization reaction. Signal amplification enhanced the sensitivity for target DNA detection. The proposed method could detect target DNA at a linear range from 1.0 pM to 70 pM, with a detection limit of 0.3 pM. The DNA sensor exhibited good stability and acceptable reproducibility. The sensor also showed selectivity against non-complementary target DNA. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:1535 / 1541
页数:7
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