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首页> 外文期刊>Analytical chemistry >Y-Shaped DNA Duplex Structure-Triggered Gold Nanoparticle Dimers for Ultrasensitive Colorimetric Detection of Nucleic Acid with the Dark-Field Microscope
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Y-Shaped DNA Duplex Structure-Triggered Gold Nanoparticle Dimers for Ultrasensitive Colorimetric Detection of Nucleic Acid with the Dark-Field Microscope

机译:Y形DNA双链体结构引发的金纳米颗粒二聚体,用于用暗场显微镜对核酸进行超敏比色探测

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src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancham/2017/ancham.2017.89.issue-23/acs.analchem.7b03391/20171129/images/medium/ac-2017-033912_0009.gif">Herein, we present a novel gold nanoparticle (AuNP) enumeration-based colorimetric aptamer biosensor for ultrasensitive detection of nucleic acid. This AuNP enumeration-based colorimetric method takes advantages of the distinctive and strong localized surface plasmon resonance light scattering with the dark-field microscope. In our model system, first, cost-effective DNA1 instead of expensive 2-thioethyl ether acetic acid was capped on the surface of AuNPs to form a dense DNA1 layer. Then, two DNA strands (DNA2 and DNA3) in two different solutions were separately asymmetrically functionalized on the AuNPs capped dense DNA1 layer. The subsequent binding of the target DNA could trigger the formation of perfect complementary DNA with a Y shape and adjust the distance between nanoparticles to form AuNP dimers, accompanied by a color change from green to yellow as observed, and thereby modulated the performance of the sensor, which resulted in the ultrahigh sensitivity. With this design, a 43 aM limit of detection was obtained, which exhibited an increase of at least 5–9 orders of magnitude in sensitivity over other colorimetric sensors fabricated using conventional strategies.
机译:src =“http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancham/2017/canham.2017.89.issue-23/acs.analchem.7b03391/20171129/images/medium /℃-2017-033912_0009.gif“witherin,我们提出了一种基于新的金纳米粒子(AUnp)枚举的比色体传感器,用于核酸的超声检测。基于AUNP枚举的比色方法采用了与暗场显微镜的独特和强局部等离子体共振光散射的优点。在我们的模型系统中,首先,经济高效的DNA1代替昂贵的2-硫代乙基醚乙酸被盖在AUNP的表面上以形成致密的DNA1层。然后,在两种不同溶液中的两种DNA链(DNA2和DNA3)在AUNPS上升致密DNA1层上单独相比官能化。靶DNA的后续结合可以触发具有Y形的完美互补DNA的形成,并调节纳米颗粒之间的距离以形成AUNP二聚体,伴随着从绿色到黄色的颜色变化,从而调制了传感器的性能,这导致了超高敏感性。利用这种设计,获得了43AM的检测限制,其在使用常规策略制造的其他比色传感器上呈现至少5-9个响度级的增加。

著录项

  • 来源
    《Analytical chemistry》 |2017年第23期|共7页
  • 作者单位

    Department of Chemistry Capital Normal University Beijing 100048 China;

    College of Chemistry and Environmental Engineering Shandong University of Science and Technology Qingdao Shandong 266510 China;

    Department of Chemistry Capital Normal University Beijing 100048 China;

    Department of Chemistry Capital Normal University Beijing 100048 China;

    Department of Chemistry Capital Normal University Beijing 100048 China;

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