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基于正电荷金纳米粒子、DNA 模板银纳米簇、T-Hg(II)-T 相互作用和外切酶辅助信号放大的汞(II)荧光测定。

Fluorometric determination of mercury(II) using positively charged gold nanoparticles, DNA-templated silver nanoclusters, T-Hg(II)-T interaction and exonuclease assisted signal amplification.

机构信息

School of Life Science, Jiangsu Normal University, Xuzhou, 221116, China.

出版信息

Mikrochim Acta. 2019 May 2;186(5):317. doi: 10.1007/s00604-019-3388-7.

Abstract

The authors describe a method for detection of Hg by using positively charged gold nanoparticles ((+)AuNPs) as a quencher of the fluorescence of DNA-capped silver nanoclusters (DNA-AgNCs) which are negatively charged. In the presence of Hg, a DNA duplex is formed through T-Hg-T coordination chemistry. The duplex can be digested by exonuclease III to form smaller DNA fragments. This leads to the release of the AgNCs and the recovery of fluorescence, best measured at excitation/emission wavelengths of 460/530 nm. The (+)AuNPs and Hg are also released and can be reused for target recycling signal amplification. Based on these findings, a method is worked out for the determination of Hg that works in the 5.0 pM to 10 nM concentration range and has a detection limit as low as 2.3 pM. It is highly selective because of the highly specific formation of T-Hg-T bonds. Graphical abstract By using ultrastable and positively charged gold nanoparticles as fluorescence quenchers and exonuclease assisted signal amplification, a method is developed for the sensitive and selective detection of Hg in water samples.

摘要

作者描述了一种通过使用带正电荷的金纳米粒子(+AuNPs)作为荧光猝灭剂来检测 Hg 的方法,带负电荷的 DNA 封端的银纳米团簇(DNA-AgNCs)会被其猝灭。在 Hg 存在的情况下,通过 T-Hg-T 配位化学形成 DNA 双链体。双链体可以被核酸外切酶 III 消化,形成更小的 DNA 片段。这导致 AgNCs 的释放和荧光的恢复,在激发/发射波长为 460/530nm 时测量最佳。+AuNPs 和 Hg 也被释放出来,可以被重新用于目标循环信号放大。基于这些发现,开发了一种用于测定 Hg 的方法,其在 5.0 pM 至 10 nM 浓度范围内有效,检测限低至 2.3 pM。由于 T-Hg-T 键的高度特异性形成,该方法具有高度选择性。

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