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Ultrasensitive Electrochemiluminescence Biosensor for Speedy Detection of microRNA Based on a DNA Rolling Machine and Target Recycling

机译:超敏感的电化学发光生物传感器,用于基于DNA轧机的MicroRNA和目标再循环

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摘要

Intelligent DNA walking machines have become a great hot spot in biosensing, but the walking efficiency of DNA walking machines was still limited due to the low local concentration of substance DNA and the derail of leg DNA. Herein, a Zn2+-driven DNA rolling machine was proposed to overcome the above shortages and applied as a electrochemiluminescence (ECL) biosensor for speedy ultra sensitive detection of microRNA-21. First, the original DNA rolling machine was synthesized by numbers of leg DNA modified on Au nanoparticle which matched with the high concentration of track DNA on the sensing platform and could roll efficiently through Zn2+ driving. By this way the DNA rolling machine not only increased the local concentration of leg DNA and track DNA to improve walking efficiency but also changed the motion mode from step-by-step walking to high-speed rolling, weakening the derailment of leg DNA and shortening the moving time. Second, target induced recycling and acid dissolution could convert a finite amount of target microRNA into a large amount of Zn2+, which greatly improved the sensitivity of biosensor and overcame the drawbacks of enzyme cleavage or polymerization in common nucleic acid amplification methods. Lastly, the obtained Zn2+ was employed to drive the DNA rolling machine through specific sites recognizing and track DNA cutting to remove a quencher of ferrocene, recovering ECL emission of CdS:Mn QDs for microRNA-21 detection with a detection limit of 0.28 fM. Besides, the biosensor was successfully applied in microRNA-21 analysis from human cancer cell lysates, offered a controllable and ultrasensitive strategy for speedy detection of microRNA, and revealed a new avenue for clinical analyses.
机译:智能DNA步行机已成为生物传感的一个很大的热点,但由于物质DNA的局部浓度和腿部DNA的脱发,DNA步行机的步行效率仍然有限。在此,提出了一种Zn2 + -Drive DNA轧制机以克服上述短缺并用作电化学发光(ECL)生物传感器,用于微小RORNA-21的速度超敏检测。首先,原始的DNA滚动机由在Au纳米粒子上修饰的腿部DNA合成,其与传感平台上的高浓度的轨道DNA匹配,并且可以通过Zn2 +驱动滚动。通过这种方式,DNA滚动机不仅增加了腿部DNA的局部浓度并跟踪DNA以提高行走效率,而且还将运动模式从逐步走向高速滚动,削弱了腿部DNA的脱轨和缩短移动时间。其次,靶诱导的再循环和酸溶解可以将有限量的靶微小瘤转化为大量Zn2 +,这大大提高了生物传感器的敏感性并克服了酶裂解或常见核酸扩增方法的缺点。最后,所获得的Zn2 +用于通过识别和追踪DNA切割的特定位点驱动DNA轧机以除去二茂铁的猝灭剂,回收CDS的ECL发射:Mn QDS用于MicroRNA-21检测,检测限为0.28 fm的检测。此外,生物传感器已成功应用于人癌细胞裂解物的MicroRNA-21分析中,提供了一种可控和超细策略,用于迅速检测MicroRNA,并揭示了新的临床分析途径。

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  • 来源
    《Analytical chemistry》 |2019年第7期|共6页
  • 作者单位

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Minist Educ Key Lab Luminescent &

    Real Time Analyt Chem Chongqing 400715 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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