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发布时间：2019-03-13

论文类型：期刊论文

发表时间：2015-03-21

发表刊物：ANALYST

收录刊物：Scopus、SCIE、PubMed

卷号：140

期号：6

页面范围：2029-2036

ISSN号：0003-2654

摘要：An ultrasensitive methodology was successfully developed for the quantitative detection of picomolar Hg2+ based on the combination of thymine-Hg2+-thymine (T-Hg2+-T) coordination chemistry and exonuclease III-aided recycling signal amplification. Single-strand probe DNA was immobilized on an Au electrode via an Au-S bond. In the presence of Hg2+, the probe DNA hybridized with the target DNA containing four thymine-thymine (T-T) mismatches via the Hg2+-mediated coordination of T-Hg2+-T base pairs. Then the probe DNA in the DNA duplex was specifically recognized and selectively digested by exonuclease III; in contrast the target DNA was safely dissociated from the DNA duplexes to subsequently hybridize with a new signal probe, leading to target recycling and signal amplification. As a result, the peak current caused by the electrostatic interactions of [Ru(NH3)(6)](3+) cations with the backbone of the probe DNA decreased by different degrees, corresponding to the Hg2+ concentrations. Under the optimum conditions, the proposed electrochemical DNA biosensor showed a robust detection limit as low as 1 pM (S/N = 3), with a wide linear range from 0.01 to 500 nM and good selectivity. In addition, the proposed method was successfully applied to assay Hg2+ in real environmental samples.