Ultrasensitive electrochemical sensor for mercury (II) based on target-induced structure-switching DNA

• Published in: Biosensors & bioelectronics Vol. 25; no. 5; pp. 1025 - 1031
• Main Authors: Wu, Danhong, Zhang, Qing, Chu, Xia, Wang, Haibo, Shen, Guoli, Yu, Ruqin
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier B.V 15.01.2010; Elsevier
• Subjects: Biological and medical sciences; Biosensing Techniques - instrumentation; Biotechnology; Differential pulse voltammetry; DNA - chemistry; Electrochemical sensor; Electrochemistry - instrumentation; Electrodes; Equipment Design; Equipment Failure Analysis; Fundamental and applied biological sciences. Psychology; Mercury; Mercury - analysis; Microchemistry - instrumentation; Reproducibility of Results; Sensitivity and Specificity; Structure-switching DNA; Structure-switching DNA; Electrochemical sensor; Mercury; Differential pulse voltammetry; Target; Detector; Targeting; DNA; Electrochemistry; Voltammetry; Structure
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2009.09.017

A novel electrochemical sensor has been developed for sensitive and selective detection of mercury (II) based on target-induced structure-switching DNA. A 33-mer oligonucleotide 1 with five self-complementary base pairs separated by seven thymine–thymine mismatches was first immobilized on the electrode via self-assembly of the terminal thiol moiety and then hybridized with a ferrocene-tagged oligonucleotide 2, leading to a high redox current. In the presence of Hg 2+, mercury-mediated base pairs (T–Hg 2+–T) induced the folding of the oligonucleotide 1 into a hairpin structure, resulting in the release of the ferrocene-tagged oligonucleotide 2 from the electrode surface with a substantially decreased redox current. The response characteristics of the sensor were thoroughly investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). The effect of the reaction temperature on the response of the sensor was also studied in detail. The results revealed that the sensor showed sensitive response to Hg 2+ in a concentration range from 0.1 nM to 5 μM with a detection limit of 0.06 nM. In addition, this strategy afforded exquisite selectivity for Hg 2+ against other environmentally related metal ions, which was superior to that of previous anodic stripping voltammetry (ASV)-based techniques. The excellent sensitivity and selectivity signified the potential of the sensor for Hg 2+ detection in real environmental samples.