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通过双足DNA步行器在电极表面逐步移动实现高效链置换扩增用于抗生素的超灵敏检测。

Efficient strand displacement amplification via stepwise movement of a bipedal DNA walker on an electrode surface for ultrasensitive detection of antibiotics.

作者信息

Zhang Rufeng, Zhang Jie, Qu Xiaonan, Li Shasha, Zhao Yihan, Liu Su, Wang Yu, Huang Jiadong, Yu Jinghua

机构信息

School of Water Conservancy and Environment, University of Jinan, Jinan 250022, P.R. China.

College of Biological Sciences and Technology, University of Jinan, Jinan 250022, P.R. China.

出版信息

Analyst. 2020 Apr 14;145(8):2975-2981. doi: 10.1039/d0an00139b.

Abstract

DNA walkers, one of the artificial molecular machines which are constructed via smart synthetic DNA, have attracted rapidly growing attention from researchers in the biosensing field. In this work, we design an Exonuclease III (Exo III)-aided target-aptamer binding recycling (ETBR) activated bipedal DNA machine for highly sensitive electrochemical detection of antibiotics. To the best of our knowledge, this is the first time that a bipedal DNA machine has been applied in electrochemical sensing for antibiotics. On the one hand, the bipedal DNA walker exceeds the conventional single swing arm DNA walker in terms of walking efficiency and stability. On the other hand, the ETBR strategy, along with efficient strand displacement amplification via stepwise movement of a bipedal DNA walker significantly promotes the signal amplification efficiency. Under optimal conditions, this bipedal DNA machine possesses a detection limit of 7.1 fM within a linear detection range from 10 fM to 100 pM. Moreover, this electrochemical biosensor is expected to detect a wide variety of analytes using the corresponding target recognition probes. Thus, our proposed strategy offers a highly efficient, stable and practical platform for small molecule analysis.

摘要

DNA步行器是通过智能合成DNA构建的人工分子机器之一,已迅速引起生物传感领域研究人员越来越多的关注。在这项工作中,我们设计了一种由核酸外切酶III(Exo III)辅助的靶适配体结合循环(ETBR)激活的双足DNA机器,用于抗生素的高灵敏度电化学检测。据我们所知,这是双足DNA机器首次应用于抗生素的电化学传感。一方面,双足DNA步行器在行走效率和稳定性方面超过了传统的单摆臂DNA步行器。另一方面,ETBR策略与通过双足DNA步行器的逐步移动进行的高效链置换扩增一起,显著提高了信号放大效率。在最佳条件下,这种双足DNA机器在10 fM至100 pM的线性检测范围内具有7.1 fM的检测限。此外,这种电化学生物传感器有望使用相应的靶标识别探针检测多种分析物。因此,我们提出的策略为小分子分析提供了一个高效、稳定且实用的平台。

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