...
首页> 外文期刊>Analytical chemistry >A Target-Triggered DNAzyme Motor Enabling Homogeneous, Amplified Detection of Proteins
【24h】

A Target-Triggered DNAzyme Motor Enabling Homogeneous, Amplified Detection of Proteins

机译:靶触发的DNAzyme电机,可实现均匀,扩增检测蛋白质

获取原文
获取原文并翻译 | 示例
           

摘要

src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancham/2017/ancham.2017.89.issue-23/acs.analchem.7b03529/20171206/images/medium/ac-2017-03529s_0005.gif">We report here the concept of a self-powered, target-triggered DNA motor constructed by engineering a DNAzyme to adapt into binding-induced DNA assembly. An affinity ligand was attached to the DNAzyme motor via a DNA spacer, and a second affinity ligand was conjugated to the gold nanoparticle (AuNP) that was also decorated with hundreds of substrate strands serving as a high-density, three-dimensional track for the DNAzyme motor. Binding of a target molecule to the two ligands induced hybridization between the DNAzyme and its substrate on the AuNP, which are otherwise unable to spontaneously hybridize. The hybridization of DNAzyme with the substrate initiates the cleavage of the substrate and the autonomous movement of the DNAzyme along the AuNP. Each moving step restores the fluorescence of a dye molecule, enabling monitoring of the operation of the DNAzyme motor in real time. A simple addition or depletion of the cofactor Mg2+ allows for fine control of the DNAzyme motor. The motor can translate a single binding event into cleavage of hundreds of substrates, enabling amplified detection of proteins at room temperature without the need for separation.
机译:src =“http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancham/2017/acham.2017.89.issue-23/acs.analchem.7b03529/20171206/images/medium /ac-2017-03529S_0005.gif">我们在此报告通过工程为DNAzyme构建的自动,目标触发DNA电动机的概念,以适应结合诱导的DNA组件。通过DNA间隔物连接到DNAzyme电动机上的亲和配体,第二个亲和配体与金纳米颗粒(AUNP)缀合,该金纳米粒子(AUNP)也用数百个衬底股线装饰,用作高密度,三维轨道DNazyme电机。靶分子与两种配体的结合诱导DNAzyme及其基材在AUNP上的杂交,否则不能自发地杂交。 DNAzyme与底物的杂交引发了衬底的切割和沿着AUNP的DNAzyme的自主运动。每个移动步骤恢复染料分子的荧光,能够实时监测DNAzyme电机的操作。辅因子Mg 2 + 的简单添加或耗尽允许对DNAzyme电机进行微量的控制。电动机可以将单个结合事件转化为数百个底物的切割,使得在室温下能够放大蛋白质,而不需要分离。

著录项

  • 来源
    《Analytical chemistry》 |2017年第23期|共8页
  • 作者单位

    Analytical and Testing Center Sichuan University 29 Wangjiang Road Chengdu Sichuan 610064 China;

    Division of Analytical and Environmental Toxicology Department of Laboratory Medicine and Pathology Faculty of Medicine and Dentistry University of Alberta Edmonton Alberta T6G 2G3 Canada;

    Division of Analytical and Environmental Toxicology Department of Laboratory Medicine and Pathology Faculty of Medicine and Dentistry University of Alberta Edmonton Alberta T6G 2G3 Canada;

    Division of Analytical and Environmental Toxicology Department of Laboratory Medicine and Pathology Faculty of Medicine and Dentistry University of Alberta Edmonton Alberta T6G 2G3 Canada;

    Analytical and Testing Center Sichuan University 29 Wangjiang Road Chengdu Sichuan 610064 China;

    Division of Analytical and Environmental Toxicology Department of Laboratory Medicine and Pathology Faculty of Medicine and Dentistry University of Alberta Edmonton Alberta T6G 2G3 Canada;

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

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号