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首页> 外文期刊>Sensors and Actuators >Design of metal-ion-triggered assembly of label-free split G-quadruplex/duplex DNA for turn-on detection of Hg~(2+) in fetal calf serum
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Design of metal-ion-triggered assembly of label-free split G-quadruplex/duplex DNA for turn-on detection of Hg~(2+) in fetal calf serum

机译:金属离子触发的无标记分裂G-四链体/双链体DNA的装配设计,用于胎牛血清中Hg〜(2+)的开启检测

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摘要

A simple oligonucleotide-based label-free turn-on fluorescent Hg~(2+) sensor depending on the transformation of the random single-stranded DNA (ssDNA) into a G-quadruplex/double-stranded DNA (dsDNA) assemble has been developed. The proposed sensor combines the advantages of the huge enhancement of Thioflavin T binding to G-quadruplex/dsDNA assemble and high selectivity of the thymine (T)-T mismatched base pairs to Hg~(2+). In the presence of Hg~(2+), the two separated ssDNA prefer to form a metal-dsDNA complex, which results in the two G-rich segments connecting to each other and forming a split G-quadruplex complex. First, the reporter ThT bind to the G-quadruplex and then intercalate to dsDNA, resulting in remarkable fluorescence enhancement (~16-fold). The sensor affords a high sensitivity for Hg~(2+), with a low limit of detection (LOD) of 10 nM based on a calculation of 3cr/slope. The main features of the proposed sensor include: (1) Simple design and easy operation, (2) the proposed sensor displays high sensitivity and lower limit of detection for Hg~(2+). (3) Environmental friendly and being used for assessing Hg~(2+) levels in fetal calf serum (FCS) with satisfactory results.
机译:基于随机单链DNA(ssDNA)转化为G-四链体/双链DNA(dsDNA)组装体的简单的基于寡核苷酸的无标记开启荧光Hg〜(2+)传感器已经开发出来。 。拟议的传感器结合了硫黄素T与G-四链体/ dsDNA组装的结合大大增强以及胸腺嘧啶(T)-T错配碱基对Hg〜(2+)的选择性高的优点。在存在Hg〜(2+)的情况下,两个分离的ssDNA倾向于形成金属-dsDNA复合物,这导致两个富含G的区段彼此连接并形成分裂的G-四链体复合物。首先,报道分子ThT与G-四链体结合,然后插入dsDNA,导致显着的荧光增强(约16倍)。该传感器对Hg〜(2+)具有很高的灵敏度,基于3cr /斜率的计算,其检测下限(LOD)为10 nM。提出的传感器的主要特点包括:(1)设计简单,操作简便;(2)提出的传感器对Hg〜(2+)具有较高的灵敏度和较低的检测限。 (3)对环境友好,可用于评估胎牛血清(FCS)中Hg〜(2+)的水平,效果令人满意。

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  • 来源
    《Sensors and Actuators》 |2018年第1期|1024-1030|共7页
  • 作者单位

    Lab of Biosystem and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science & Technology, Shanghai, 200237 China;

    Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engeering, Shangqiu Normal University, Shangqiu, 476000, China;

    College of Chemistry and Molecular Engeering, Zhengzhou University, Zhengzhou, 450001, China;

    College of Chemistry and Material Science, Huaibei Normal University, Huaibei, 235000, China;

    Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engeering, Shangqiu Normal University, Shangqiu, 476000, China,College of Chemistry and Material Science, Huaibei Normal University, Huaibei, 235000, China;

    Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engeering, Shangqiu Normal University, Shangqiu, 476000, China;

    Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engeering, Shangqiu Normal University, Shangqiu, 476000, China;

    Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engeering, Shangqiu Normal University, Shangqiu, 476000, China,College of Chemistry and Molecular Engeering, Zhengzhou University, Zhengzhou, 450001, China;

    Lab of Biosystem and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science & Technology, Shanghai, 200237 China;

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

    G-quadruplex/duplex DNA; Label-free; Turn-on fluorescence; Hg~(2+);

    机译:G-四链体/双链体DNA;无标签;开启荧光;汞〜(2+);

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