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首页> 外文期刊>Sensors and Actuators >Electrode immobilization-free and sensitive electrochemical sensing of thrombin via magnetic nanoparticle-decorated DNA polymers
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Electrode immobilization-free and sensitive electrochemical sensing of thrombin via magnetic nanoparticle-decorated DNA polymers

机译:通过磁性纳米颗粒装饰DNA聚合物的凝血酶固定和敏感电化学感测的电极固定化和敏感的电化学传感

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摘要

The development of sensitive and simple sensing strategies for trace proteins has received increasing attentions in the diagnosis and treatment of diseases. We describe here an electrode immobilization-free and homogeneous electrochemical method for sensitively detecting thrombin in human serums. The strategy relies on target-promoted proximity binding hybridization chain reaction (HCR) formation of magnetic nanoparticle (MNP)-decorated DNA polymers. Simultaneous binding of thrombin by two distinct aptamers increases their local concentrations and enables the proximity binding-induced strand displacement reaction, which leads to subsequent initiation of HCR between the methylene blue (MB)- and biotin-labeled hairpins into long DNA polymers. The streptavidin-modified MNPs further bind the biotin moieties to form the MNPs/DNA polymers. Subsequent accumulation of the MNPs/DNA polymers on the AuNP-deposited electrode can thus yield substantially enhanced current, due to the oxidation of the many MB labels, for highly sensitive detection of thrombin ranging from 5 pM~50 nM with a detection limit of 1.1 pM in a simple electrode immobilization-free way. Selective interrogation of low levels of thrombin in diluted human serums was also verified, revealing its potential for convenient and ultrasensitive monitoring of a variety of protein biomarkers for disease diagnosis at the early stages.
机译:追踪蛋白质敏感和简单的感测策略的发展得到了疾病诊断和治疗的增加。这里在此描述一种用于敏感地检测人血清中凝血酶的电极固定和均匀的电化学方法。该策略依赖于磁性纳米粒子(MNP) - 研磨的DNA聚合物的目标促进的接近结合杂交链反应(HCR)。两个不同的适体的凝血酶同时结合增加它们的局部浓度并使邻近结合诱导的链位移反应导致随后在亚甲基蓝(MB) - 和生物素标记的发夹之间的HCR在长DNA聚合物之间启动。链霉抗生物素蛋白改性的MNP进一步结合生物素部分以形成MNP / DNA聚合物。因此,由于许多MB标记的氧化,因此可以屈服于αUPP沉积电极上的MnP / DNA聚合物的累积,从而屈服,由于许多MB标签的氧化,对于从5μm〜50nm的凝血酶的高敏感性检测,检测限为1.1 PM在一个简单的电极固定的方式。还验证了在稀释的人血清中的低水平凝血酶的选择性询问,揭示了其对早期阶段疾病诊断的各种蛋白质生物标志物的方便和超细管监测的潜力。

著录项

  • 来源
    《Sensors and Actuators 》 |2021年第3期| 129395.1-129395.7| 共7页
  • 作者单位

    Key Laboratory of Luminescence Analysis and Molecular Sensing Ministry of Education School of Chemistry and Chemical Engineering Southwest University Chongqing 400715 PR China;

    Key Laboratory of Luminescence Analysis and Molecular Sensing Ministry of Education School of Chemistry and Chemical Engineering Southwest University Chongqing 400715 PR China;

    School of Chemistry and Chemical Engineering Chongqing University of Technology Chongqing 400054 PR China;

    Key Laboratory of Luminescence Analysis and Molecular Sensing Ministry of Education School of Chemistry and Chemical Engineering Southwest University Chongqing 400715 PR China;

    Key Laboratory of Luminescence Analysis and Molecular Sensing Ministry of Education School of Chemistry and Chemical Engineering Southwest University Chongqing 400715 PR China;

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

    Aptamer; Hybridization chain reaction; Electrochemical assay; Signal amplification; Thrombin;

    机译:适体;杂交链反应;电化学测定;信号放大;凝血酶;

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