Electrocatalytic assay of mercury(II) ions using a bifunctional oligonucleotide signal probe

被引:30
|
作者
Zhang, Ziping [1 ,2 ]
Yin, Jungang [2 ]
Wu, Zhaoyang [1 ]
Yu, Ruqin [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[2] Yantai Univ, Coll Life Sci, Yantai 264005, Peoples R China
基金
中国国家自然科学基金;
关键词
Mercury; Oligonucleotide probe; Electrocatalytic amplification; Electrochemical biosensor; COLORIMETRIC DETECTION; SELECTIVE DETECTION; DNA; HG2+; DNAZYME; SENSOR;
D O I
10.1016/j.aca.2012.12.008
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Engineered nucleic acid probes containing recognition and signaling functions find growing interest in biosensor design. In this paper, we developed a novel electrochemical biosensor for sensitive and selective detecting of Hg2+ based on a bifunctional oligonucleotide signal probe combining a mercury-specific sequence and a G-quadruplex (G4) sequence. For constructing the electrochemical Hg2+ biosensor, a thiolated, mercury-specific oligonucleotide capture probe was first immobilized on gold electrode surface. In the presence of Hg2+, a bifunctional oligonucleotide signal probe was hybridized with the immobilized capture probe through thymine-mercury(II)-thymine interaction-mediated surface hybridization. The further interaction between G4 sequence of the signal probe and hemin generated a G4-hemin complex, which catalyzed the electrochemical reduction of hydrogen peroxide, producing amplified readout signals for Hg2+ interaction events. This electrochemical Hg2+ biosensor was highly sensitive and selective to Hg2+ in the concentration of 1.0 nM to 1 mu M with a detection limit of 0.5 nM. The new design of bifunctional oligonucleotide signal probes also provides a potential alternative for developing simple and effective electrochemical biosensors capable of detecting other metal ions specific to natural or artificial bases. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 53
页数:7
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