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Mercury-DNA interaction based detection of mercury ions by DNA amplification with high sensitivity and selectivity

机译:基于汞-DNA相互作用的DNA扩增基于汞离子的检测,具有高灵敏度和选择性

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摘要

An effective and facile approach for mercury detection is essential for environmental protection and human health. In this study, we propose a novel strategy to develop a highly sensitive and selective method for the detection of mercury ions using real-time quantitative polymerase chain reaction (RT-qPCR) technology and the specific binding of Hg2+ in thymine-thymine mismatch complexes. The signal for detection of Hg2+ was generated using RT-qPCR amplification of a template strand of DNA. The sensor exhibited an excellent linear response between the cycle threshold (Ct) and mercury ion concentration in the range of 0.05-100 nM. Under optimised conditions, the detection limit of this method for aqueous Hg2+ was as low as 30 pM. In addition, this system showed good selectivity for Hg2+ over other metal ions. This new approach shows significant potential for detection of Hg2+ in water and other samples.
机译:有效且汞检测方法对于环境保护和人类健康至关重要。 在这项研究中,我们提出了一种新的策略,用于使用实时定量聚合酶链反应(RT-QPCR)技术和HG2 +在胸腺嘧啶 - 胸腺嘧啶混合物中HG2 +的特异性结合来开发一种高敏感和选择性的方法。 使用DNA的模板链的RT-QPCR扩增产生用于检测HG2 +的信号。 在0.05-100nm的范围内,传感器在循环阈值(CT)和汞离子浓度之间表现出优异的线性响应。 在优化条件下,该方法HG2 +水溶液的检测极限为低至30μm。 此外,该系统对其他金属离子的HG2 +显示出良好的选择性。 这种新方法显示出在水和其他样品中检测HG2 +的显着潜力。

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