首页> 外文期刊>Sensors and Actuators >A label-free and enzyme-free fluorescent assay for mercury ions based on T-Hg(Ⅱ)-T nanoladders and DNA-templated silver nanoclusters/graphene oxide nanocomposites
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A label-free and enzyme-free fluorescent assay for mercury ions based on T-Hg(Ⅱ)-T nanoladders and DNA-templated silver nanoclusters/graphene oxide nanocomposites

机译:基于T-Hg(Ⅱ)-T纳米酰胺和DNA模板银纳米蛋白/石墨烯纳米复合材料的无汞离子的无标记和酶无酶荧光测定

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摘要

A label-free and enzyme-free signal-on biosensor for Hg(Ⅱ) ions was constructed based on T-Hg(Ⅱ)-T nanoladders and fluorescent DNA-templated silver nanoclusters/graphene oxide nanocomposites (DNA-AgNCs/GO). The T-rich sequences (P1 and P2) were used to capture Hg(Ⅱ) and form the T-Hg(Ⅱ)-T nanoladders. C_6G_5C_6 was extended at the 5' end of PI, used as a template for synthesizing fluorescent DNA-AgNCs. In the presence of mercury ions, the T-Hg(Ⅱ)-T nanoladders significantly enhanced the emission of AgNCs. GO can attract free P1-C_6G_5C_6 and P2 that were not involved in the formation of T-Hg(Ⅱ)-T nanoladders, thus employed as the energy acceptor to quench the background fluorescence of AgNCs. The fluorescence enhancement induced by mercury ions can be used for quantitative detection of Hg(Ⅱ) over the range 0.1-30 nM with a detection limit as low as 7.35 pM. This method was used to detect Hg(Ⅱ) in the spiked samples of Songhua River water and grass carp, with the recoveries of 97.61%- 103.79% and 96.52%- 105.58% respectively, consistent with the results from atomic fluorescence spectrometry. Obviously, in this assay, enzyme-free signal amplification and signal identification are integrated in the ingenious design of nucleic acid sequences, thus achieving the label-free fluorescence detection of mercury ions.
机译:基于T-Hg(Ⅱ)-T纳米辐射剂和荧光DNA模板银纳米蛋白/石墨烯纳米复合材料(DNA-AGNCS / GO),构建了用于HG(Ⅱ)离子的无标记和酶的信号生物传感器。富含T的序列(P1和P2)用于捕获Hg(Ⅱ)并形成T-Hg(Ⅱ)-T纳米乳糖。 C_6G_5C_6在PI的5'末端延伸,用作合成荧光DNA-AGNC的模板。在汞离子的存在下,T-Hg(Ⅱ)-T纳米辐射剂显着增强了AGNC的排放。 GO可以吸引不参与T-Hg(Ⅱ)-T纳米乳糖的形成的游离P1-C_6G_5C_6和P2,从而采用能量受体来淬灭AGNC的背景荧光。由汞离子诱导的荧光增强可用于定量检测0.1-30nm范围内的Hg(Ⅱ),检测限为低至7.35μm。该方法用于检测松花河水和草鲤鱼的尖刺样品中的Hg(Ⅱ),其回收率分别为97.61% - 103.79%和96.52% - 105.58%,与原子荧光光谱法的结果一致。显然,在该测定中,在核酸序列的巧妙设计中,无酶信号放大和信号鉴定集成在核酸序列的巧妙设计中,从而达到无汞离子的无标记荧光检测。

著录项

  • 来源
    《Sensors and Actuators》 |2021年第12期|130707.1-130707.11|共11页
  • 作者单位

    Department of Food Quality and Safety College of Food Science and Engineering Electron Microscopy Center Jilin University Changchun 130062 China;

    Department of Food Quality and Safety College of Food Science and Engineering Electron Microscopy Center Jilin University Changchun 130062 China;

    Department of Food Quality and Safety College of Food Science and Engineering Electron Microscopy Center Jilin University Changchun 130062 China;

    Department of Food Quality and Safety College of Food Science and Engineering Electron Microscopy Center Jilin University Changchun 130062 China;

    Department of Food Quality and Safety College of Food Science and Engineering Electron Microscopy Center Jilin University Changchun 130062 China;

    Department of Food Quality and Safety College of Food Science and Engineering Electron Microscopy Center Jilin University Changchun 130062 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Mercury ion; Nanoladders; DNA-AgNCs; Graphene oxide; Fluorescence;

    机译:汞离子;纳米拉德斯;DNA-AGNCS;氧化石墨烯;荧光;

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