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基于熵驱动的催化反应诱导发夹结构切换的铀酰离子荧光检测。

Entropy-driven catalytic reaction-induced hairpin structure switching for fluorometric detection of uranyl ions.

机构信息

State Key Laboratory of Environment-Friendly Energy Material, Southwest University of Science and Technology, Mianyang, 621010, People's Republic of China.

School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, 325035, China.

出版信息

Mikrochim Acta. 2019 Aug 28;186(9):653. doi: 10.1007/s00604-019-3767-0.

Abstract

An ultra-sensitive and "turn-on" method is demonstrated for the determination of uranyl ion. The assay is based on hairpin-to-DNAzyme structure switching that is induced by an entropy-driven catalytic reaction. An UO-specific DNAzyme is cleaved by UO to produce a DNA fragment. This fragment initiates the entropy-driven catalytic reaction to produce a large number of a sequence "R". The sequence R initiates the circular cleavage of FAM-labeled hairpins by switching the hairpin to Mg-specific DNAzyme structure. This causes the recovery of green fluorescence. The method works in the 20 pM to 800 pM concentration range and the limit of detection is 4 pM. Graphical abstract Entropy driven catalytic reaction induced hairpin structure switching for fluorometric detection of uranyl ions.

摘要

一种超灵敏的“开启”方法被用于铀酰离子的测定。该分析方法基于发夹到 DNA 酶结构的转换,这是由熵驱动的催化反应诱导的。UO 特异性 DNA 酶被 UO 切割,产生一个 DNA 片段。该片段启动熵驱动的催化反应,产生大量的序列“R”。该序列 R 通过将发夹切换到 Mg 特异性 DNA 酶结构,引发 FAM 标记发夹的循环切割。这导致绿色荧光的恢复。该方法在 20 pM 至 800 pM 的浓度范围内有效,检测限为 4 pM。

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