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Click Chemistry Reaction-Triggered 3D DNA Walking Machine for Sensitive Electrochemical Detection of Copper Ion

机译:单击化学反应触发的3D DNA步行机,用于铜离子的敏感电化学检测

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摘要

Herein, for the first time, we engineered click chemistry reaction to trigger a 3D DNA walking machine for ultrasensitive electrochemical detection of copper ion (Cu2+), which provided a convenient access to overcome the shortcomings of poor selectivity and limited amplification efficiency in traditional determination of Cu2+. Click chemistry reaction drove azido-S2 to bind with alkynyl-S1 for the formation of a walker probe on aminated magnetic polystyrene microsphere@gold nanoparticles (PSC@Au), which opened the hairpin-locked DNAzyme. In the presence of magnesium ion (Mg2+), the unlocked DNAzyme was activated to cleave the self-strand at the facing ribonucleotide site, accompanied by the release of product DNA (S3) and the walker probe. Therefore, the walker probe was able to open the adjacent hairpin-locked DNAzyme strand and then be released by DNAzyme cleavage along the PSC@Au-DNAzyme track. Eventually, the liberated single-strand S3 induced catalytic hairpin assembly (CHA) recycling, resulting in the capture of a large number of methylene blue-tagged hairpin DNA (MB-H2) on the sensor surface and significant electrochemical responses. By coupling click chemistry reaction with the dual-amplification strategy of the 3D DNA walking machine and CHA recycling, the proposed biosensor not only demonstrated high accuracy and selectivity for Cu(2+)detection in real samples but also showed excellent performance for Cu2+ detection with a wide linear range of 1.0 pM to 500 nM and low detection limit of 0.33 pM. Moreover, this elaborated biosensor could be readily expanded to Mg2+ detection with a constant concentration of Cu2+, which paves a new way to apply the 3D DNA walking machine in various ion sensings.
机译:在此,我们首次设计了单击化学反应,以触发用于铜离子(CU2 +)的超细电化学检测的3D DNA行走机,这提供了方便的进入,以克服传统测定中的选择性差和有限扩增效率的缺点CU2 +。点击化学反应驱动Azido-S2与炔基-S1结合,用于在胺化磁聚苯乙烯微球中形成助行器探针,打开发夹锁定的DNazyme。在镁离子(Mg2 +)的存在下,被激活解锁的DNAzyme以切割面向核糖核苷酸位点的自股,伴随产物DNA(S3)和步行探针。因此,步行者探针能够打开相邻的发夹锁定的DNAzyme链,然后通过沿着PSC -DNazyme轨道的DNazyme裂解释放。最终,释放的单链S3诱导的催化发夹组件(CHA)回收,导致在传感器表面上捕获大量亚甲基蓝标记的发夹DNA(MB-H2)和显着的电化学反应。通过耦合点击化学反应3D DNA步行机的双扩增策略和CHA回收,该拟议的生物传感器不仅在真实样品中表现出Cu(2+)检测的高精度和选择性,而且还表明了Cu2 +检测的优异性能宽线性范围为1.0pm至500nm,检测限为0.33μm。此外,这种精细的生物传感器可以容易地扩展至Mg2 +检测,恒定的Cu2 +,其铺设了一种在各种离子感测中应用3D DNA行走机的新方法。

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  • 来源
    《Analytical chemistry》 |2018年第19期|共7页
  • 作者单位

    Chongqing Univ Arts &

    Sci Chongqing Key Lab Environm Mat &

    Remediat Technol Chongqing 402160 Peoples R China;

    Chongqing Univ Arts &

    Sci Chongqing Key Lab Environm Mat &

    Remediat Technol Chongqing 402160 Peoples R China;

    Chongqing Univ Arts &

    Sci Chongqing Key Lab Environm Mat &

    Remediat Technol Chongqing 402160 Peoples R China;

    Chongqing Univ Arts &

    Sci Chongqing Key Lab Environm Mat &

    Remediat Technol Chongqing 402160 Peoples R China;

    Chongqing Univ Arts &

    Sci Chongqing Key Lab Environm Mat &

    Remediat Technol Chongqing 402160 Peoples R China;

    Chongqing Vocat Inst Engn Chongqing 402260 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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