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Graphene-Assisted Label-Free Homogeneous Electrochemical Biosensing Strategy based on Aptamer-Switched Bidirectional DNA Polymerization

机译:基于适体转换双向DNA聚合的石墨烯辅助无标记均质电化学生物传感策略

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In this contribution, taking the discrimination ability of graphene over single-stranded (ss) DNA/double-stranded (ds) DNA in combination with the electrochemical impedance transducer, we developed a novel label-free homogeneous electrochemical biosensor using graphene-modified glassy carbon electrode (GCE) as the sensing platform. To convert the specific aptamer-target recognition into ultrasensitive electrochemical signal output, a novel aptamer-switched bidirectional DNA polymerization (BDP) strategy, capable of both target recycling and exponential signal amplification, was compatibly developed in this study. In this strategy, all the designed DNA structures could be adsorbed on the graphene/GCE and, thus, serve as the electrochemical impedance signal reporter, while the target acts as a trigger of this BDP reaction, in which these designed DNA structures are bound together and, then, converted to long dsDNA duplex. The distinct difference in electrochemical impedance spectroscopy between the designed structures and generated long dsDNA duplex on the graphene/GCE allows label-free and homogeneous detection of target down to femto-gram level. The target can be displaced from aptamer through the polymerization to initiate the next recognition polymerization cycle. Herein, the design and signaling principle of aptamer-switched BDP amplification system were elucidated, and the working conditions were optimized. This method not only provides a universal platform for electrochemical biosensing but also shows great potential in biological process researches and clinic diagnostics.
机译:在这项贡献中,结合电化学阻抗传感器,利用石墨烯对单链(ss)DNA /双链(ds)DNA的识别能力,我们开发了一种使用石墨烯修饰的玻璃碳的新型无标记均质电化学生物传感器电极(GCE)作为传感平台。为了将特定的适体-靶标识别转换成超灵敏的电化学信号输出,在本研究中兼容开发了一种新型的适体开关双向DNA聚合(BDP)策略,该策略能够同时进行靶标回收和指数信号放大。在这种策略中,所有设计的DNA结构都可以吸附在石墨烯/ GCE上,从而充当电化学阻抗信号报告物,而靶标则充当该BDP反应的触发,其中这些设计的DNA结构被结合在一起然后,转换为长dsDNA双链体。在设计的结构和在石墨烯/ GCE上生成的长dsDNA双链体之间的电化学阻抗谱上的显着差异,可实现无标记且均质的目标检测,直至飞克级。可以通过聚合将靶从适体中置换出来,以启动下一个识别聚合循环。阐明了适体开关的BDP放大系统的设计和信号传导原理,并优化了工作条件。该方法不仅为电化学生物传感提供了通用平台,而且在生物过程研究和临床诊断中显示出巨大潜力。

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