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A signal-on electrochemical aptasensor for highly sensitive and specific detection of kanamycin based on target-induced signaling probe shifting mechanism

机译:基于靶诱导信号探针位移机制的信号灵敏电化学适体传感器,用于卡那霉素的高灵敏度和特异性检测

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摘要

An electrochemical displacement-based aptasensor was developed for the detection of kanamycin-a (KMY-A). Based on the target-induced signaling probe shifting mechanism, this aptasensor shows a “signal on” change with a simple 3-probe structure. One no-thiolated capture probe and one thiolated assistant probe are attached onto the Au electrode surface in a short duplex state, and one methylene blue (MB)-labelled signaling probe is free in the detection solution. Before adding theKMY-A, a very small background signal is obtained with low efficient electron transfer because of theMBlabels on the signaling probe far from the electrode surface. After adding theKMY-A, the more stable capture probe/KMY-Acomplex formed between the capture probe and theKMY-Aundoes the former short duplex to release the assistant probe, which induces the formation of another assistant probe/signaling probe duplex. This structure change can shift theMBlabels close to the electrode surface with much higher efficient electron transfer, thereby leading to a big detection signal. Under the optimized fabrication and detection conditions, the sensor features a high sensitivity forKMY-Awith the detection limit of 3.3 pM and a fast sensing speed with the response time of ∼9 min. In addition, it is worth mentioning that the target discrimination ability of sensor can be improved through using longer assistant probe to strengthen the hybridization force between the capture probe and the assistant probe, which is helpful for establishing the special detection system with high specificity requirement.
机译:开发了一种基于电化学位移的适体传感器,用于检测卡那霉素-a(KMY-A)。基于靶标诱导的信号探针移位机制,该适体传感器显示了具有简单3探针结构的“信号开启”变化。一种非硫醇化的捕获探针和一种硫醇化的辅助探针以短双工状态连接到Au电极表面,并且一种亚甲基蓝(MB)标记的信号探针在检测溶液中游离。在添加KMY-A之前,由于信号探针上的MB标记远离电极表面,因此获得了非常小的背景信号,且电子转移效率较低。加入KMY-A后,在捕获探针和KMY-A之间形成的更稳定的捕获探针/ KMY-A复合体将原先的短双链体撤消以释放辅助探针,从而诱导另一个辅助探针/信号探针双链体的形成。这种结构变化可以使MB标签移动到电极表面附近,并且电子转移效率更高,从而导致检测信号大。在优化的制造和检测条件下,该传感器具有对KMY-A的高灵敏度,检测极限为3.3MpM,并且具有快速的感应速度,响应时间约为9 min。另外,值得一提的是,通过使用更长的辅助探针来增强捕获探针与辅助探针之间的杂交力,可以提高传感器的目标分辨能力,这有助于建立具有高特异性要求的特殊检测系统。

著录项

  • 来源
    《Sensors and Actuators》 |2018年第11期|480-487|共8页
  • 作者单位

    Post-Doctoral Research Center of Chongqing Key Lab of Inorganic Special Functional Materials, School of Chemistry and Chemical Engineering, Yangtze Normal University;

    Post-Doctoral Research Center of Chongqing Key Lab of Inorganic Special Functional Materials, School of Chemistry and Chemical Engineering, Yangtze Normal University,College of Chemical and Environmental Engineering, Harbin University of Science and Technology;

    Post-Doctoral Research Center of Chongqing Key Lab of Inorganic Special Functional Materials, School of Chemistry and Chemical Engineering, Yangtze Normal University,College of Chemical and Environmental Engineering, Harbin University of Science and Technology;

    Post-Doctoral Research Center of Chongqing Key Lab of Inorganic Special Functional Materials, School of Chemistry and Chemical Engineering, Yangtze Normal University;

    Post-Doctoral Research Center of Chongqing Key Lab of Inorganic Special Functional Materials, School of Chemistry and Chemical Engineering, Yangtze Normal University;

    College of Chemical and Environmental Engineering, Harbin University of Science and Technology;

    College of Chemical and Environmental Engineering, Harbin University of Science and Technology;

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

    Electrochemical aptasensor; Kanamycin; Displacement-based; Signal-on; Target-induced signaling probe shifting; Methylene blue;

    机译:电化学适体传感器;卡那霉素;基于位移;信号开启;靶标诱导的信号探针位移;亚甲基蓝;

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