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首页> 外文期刊>Analytical chemistry >Novel 2D-DNA-Nanoprobe-Mediated Enzyme-Free-Target-Recycling Amplification for the Ultrasensitive Electrochemical Detection of MicroRNA
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Novel 2D-DNA-Nanoprobe-Mediated Enzyme-Free-Target-Recycling Amplification for the Ultrasensitive Electrochemical Detection of MicroRNA

机译:新型2D-DNA-Nanopobe介导的微润松检测超细电化学检测的酶无靶 - 再循环扩增

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摘要

In this work, on the basis of a new 2D DNA nanoprobe (DNP) and an enzyme-free-target-recycling amplification, an electrochemical biosensor is developed for the ultrasensitive detection of microRNA-21 (miRNA-21). Herein, two ferrocene-labeled bipedal DNPs, which show small steric hindrance and strong stability, are prepared on the basis of the mechanism of the proximity-ligation assay (PLA), improving the space utilization. In the presence of the target, miRNA-21, and a hairpin DNA strand, the DNP will collapse, and then two ferrocene-labeled DNA strands and the miRNA-21 will be simultaneously released from the electrode surface through toehold-mediated strand-displacement reactions (TSDRs), leading to a decrease in the electrochemical signal and realization of enzyme-free target recycling. As a result, the one input target, miRNA-21, could release 2N ferrocene-labeled DNA strands, achieving a dramatic decrease in the electrochemical signal. Combining DNPs and enzyme-free target recycling, this proposed biosensor showed a linear dependence with miRNA-21 concentration, ranging from 1.0 fM to 10 nM with a detection limit of 0.31 fM. In addition, it is worth mentioning that this biosensor can be regenerated through incubating with three assistant-DNA strands, realizing the reuse of raw materials. Surprisingly, the elaborated biosensor provides a novel strategy for building controllable DNA nanoprobes for the sensitive detection of various biomarkers.
机译:在这项工作中,基于新的2D DNA纳米骨(DNP)和无酶 - 靶再循环扩增,开发了电化学生物传感器,用于微润松检测MicroRNA-21(miRNA-21)。在此,基于邻近连接测定法(PLA)的机理,提高空间利用的机理,制备两种标记的二甲双二维二对二维DNP。在靶,miRNA-21和发夹DNA链的存在下,DNP将塌陷,然后通过针兑介导的股线 - 位移同时从电极表面同时释放两个二茂铁标记的DNA链和miRNA-21反应(TSDRS),导致电化学信号的降低和无酶目标再循环的实现。结果,一种输入靶,miRNA-21可以释放2N二茂铁标记的DNA链,实现电化学信号的显着降低。组合DNP和无酶目标再循环,这一提出的生物传感器显示出与miRNA-21浓度的线性依赖性,范围为1.0 fm至10nm,检测限为0.31 fm。此外,值得一提的是,这种生物传感器可以通过与三个助助剂-DNA股线孵育来再生,实现了原料的再利用。令人惊讶的是,精心设计的生物传感器提供了一种用于构建可控DNA纳米素的新策略,用于各种生物标志物的敏感性检测。

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  • 来源
    《Analytical chemistry》 |2018年第15期|共7页
  • 作者单位

    Southwest Univ Key Lab Luminescence &

    Real Time Analyt Chem Minist Educ Coll Chem &

    Chem Engn Chongqing 400715 Peoples R China;

    Southwest Univ Key Lab Luminescence &

    Real Time Analyt Chem Minist Educ Coll Chem &

    Chem Engn Chongqing 400715 Peoples R China;

    Southwest Univ Key Lab Luminescence &

    Real Time Analyt Chem Minist Educ Coll Chem &

    Chem Engn Chongqing 400715 Peoples R China;

    Southwest Univ Key Lab Luminescence &

    Real Time Analyt Chem Minist Educ Coll Chem &

    Chem Engn Chongqing 400715 Peoples R China;

    Southwest Univ Key Lab Luminescence &

    Real Time Analyt Chem Minist Educ Coll Chem &

    Chem Engn Chongqing 400715 Peoples R China;

    Southwest Univ Key Lab Luminescence &

    Real Time Analyt Chem Minist Educ Coll Chem &

    Chem Engn 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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