Fabrication of DNA/graphene/polyaniline nanocomplex for label-free voltammetric detection of DNA hybridization

被引:68
作者
Du, Meng [1 ]
Yang, Tao [1 ]
Li, Xiao [1 ]
Jiao, Kui [1 ]
机构
[1] Qingdao Univ Sci & Technol, Shandong Prov Key Lab Biochem Anal, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphene; Polyaniline; DNA hybridization; Voltammetry; Electrochemical reduction; CARBON NANOTUBES; GRAPHENE NANOSHEETS; COMPOSITE; MOLECULES; ELECTRODE; PLATFORM; FILMS; BIOSENSOR; SENSOR; OXIDE;
D O I
10.1016/j.talanta.2011.10.054
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
A novel DNA electrochemical biosensor was described for the detection of specific gene sequences. Electrochemically reduced graphene oxide (ERGNO) was prepared on polyaniline (PAN) nanofibers modified glassy carbon electrode (GCE). Compared with the electrochemical reduction of graphene oxide directly on bare GCE (reduction potential: ca. -1.3 V), more positive reduction potential (ca. -1 V) for graphene oxide was observed with the PAN membrane existing. The formed ERGNO/PAN nanocomposites were applied to bind ssDNA probe via the non-covalent assembly. The surface density of ssDNA was calculated by voltammetric studies of redox cations ([Ru(NH3)(6)](3+)), which were bound to the surface via electrostatic interaction with negative charged phosphate backbone of the DNA. After the hybridization of ssDNA probe with complementary DNA, the response of surface-bound [Ru(NH3)(6)](3+) changed obviously, which could been adopted to recognize the DNA hybridization. Under optimal conditions, the dynamic range of the DNA biosensor for detecting the sequence-specific DNA of cauliflower mosaic virus (CaMV35S) gene was from 1.0 x 10(-13) to 1.0 x 10(-7) mol L-1, with a detection limit of 3.2 x 10(-14) mol L-1. This biosensor also showed a high degree of selectivity. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:439 / 444
页数:6
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