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基于胞嘧啶-银(I)-胞嘧啶配对形成、DNA 组装以及多组分 DNA 酶的“与”逻辑运算对银(I)的荧光检测

Fluorometric detection of silver(I) using cytosine-Ag(I)-cytosine pair formation, DNA assembly and the AND logic operation of a multiple-component DNAzyme.

机构信息

Department of Laboratory Medicine, Guizhou Provincial People's Hospital, Guiyang, 550002, China.

Department of Endocrinology, Chongqing Three Gorges Central Hospital, Chongqing, 404000, China.

出版信息

Mikrochim Acta. 2019 Jul 10;186(8):522. doi: 10.1007/s00604-019-3615-2.

DOI:10.1007/s00604-019-3615-2
PMID:31292764
Abstract

A nonenzymatic fluorometric assay is described for highly sensitive and selective detection of silver ion. It is making use of a controlled DNA assembly and an AND logic operation of a multiple-component DNAzyme (MNAzyme). It corresponds to an Ag(I)-responsive three-way junction (3-WJ) assembly. The tailored probes of the 3-WJ architecture were designed with complementary domains for subsequent assembly. Cytosine (C)-cytosine mismatches at one-way junction were set as the sensing element for Ag(I). Upon exposure to Ag(I) as an input, C-Ag(I)-C pairs are being formed. This enhances the binding energy between these separate probes and thus promotes the formation of a nanostructure that represents an AND logic assembly of MNAzyme with an amplified output signal. This results in an Ag(I)-induced increase in fluorescence which is measured best at excitation/emission maxima of 645/670 nm. The method displays high selectivity and sensitivity, has a 5 pM detection limit at 3σ and a dynamic range that extends from 10 pM to 100 nM. Graphical abstract Schematic presentation of a new fluorescence system for determining silver ion by making use of cytosine-Ag(I)-cytosine pair formation, precisely-controlled DNA assembly and "AND" logic operation of multiple components DNAzyme (MNAzyme).

摘要

一种非酶荧光测定法被描述用于高灵敏度和选择性检测银离子。它利用受控的 DNA 组装和多个组分 DNA 酶(MNAzyme)的“与”逻辑运算。它对应于 Ag(I)响应的三链结(3-WJ)组装。3-WJ 结构的定制探针设计有互补结构域,以便随后进行组装。单向结处的胞嘧啶(C)-胞嘧啶错配被设置为 Ag(I)的传感元件。暴露于 Ag(I)作为输入时,形成 C-Ag(I)-C 对。这增强了这些单独探针之间的结合能,从而促进了纳米结构的形成,该纳米结构代表了具有放大输出信号的 MNAzyme 的“与”逻辑组装。这导致 Ag(I)诱导的荧光增加,在 645/670nm 的激发/发射最大值处测量最佳。该方法具有高选择性和灵敏度,在 3σ 时检测限为 5 pM,动态范围从 10 pM 扩展到 100 nM。

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