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基于催化发夹组装和熵驱动催化级联扩增电路的可编程电化学生物传感平台。

Programmable electrochemical biosensing platform based on catalytic hairpin assembly and entropy-driven catalytic cascade amplification circuit.

机构信息

Key Laboratory of the Evaluation and Monitoring of Southwest Land Resources (Sichuan Normal University), Ministry of Education, College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, 610066, China.

Key Laboratory of the Evaluation and Monitoring of Southwest Land Resources (Sichuan Normal University), Ministry of Education, College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, 610066, China.

出版信息

Anal Chim Acta. 2023 Oct 16;1278:341715. doi: 10.1016/j.aca.2023.341715. Epub 2023 Aug 14.

Abstract

Herein, powerful DNA strand displacement reaction and sensitive electrochemical analysis method were ingeniously integrated to develop a programmable biosensing platform. Using DNA as the detection model, a cascade amplification system based on catalytic hairpin assembly and entropy-driven catalytic was constructed, and the reaction rate and signal amplification effect were significantly improved. The product of the cascade amplification circuit could undergo strand displacement reaction with the signal probe on the electrode surface to obtain sensitive electrochemical signal changes and realize highly sensitive detection of the target. In addition, without redesigning the DNA sequences in the cascade amplification circuit, the by-product strand typically wasted in traditional entropy-driven catalytic reactions can be fully utilized to construct a single-signal output biosensing system and even a dual-signal output ratiometric biosensing platform, improving the detection repeatability and reliability of the system, and expanding the application of DNA strand displacement reaction in electrochemical biosensing. Furthermore, benefiting from the design flexibility of the DNA molecules, the constructed biosensing platform realized the sensitive detection of aptamer substrate (kanamycin as an example) and certain metal ion (mercury as an example) by simply recoding the corresponding recognition sequence, demonstrating the good versatility of the biosensing platform.

摘要

本文巧妙地集成了强大的 DNA 链置换反应和灵敏的电化学分析方法,开发了一种可编程的生物传感平台。以 DNA 为检测模型,构建了基于催化发夹组装和熵驱动催化的级联放大系统,显著提高了反应速率和信号放大效果。级联放大电路的产物可以与电极表面上的信号探针进行链置换反应,以获得灵敏的电化学信号变化,从而实现对目标物的高灵敏度检测。此外,无需重新设计级联放大电路中的 DNA 序列,通常在传统的熵驱动催化反应中浪费的副产物链可以被充分利用来构建单信号输出生物传感系统,甚至构建双信号输出比率型生物传感平台,从而提高了系统的检测重复性和可靠性,并扩展了 DNA 链置换反应在电化学生物传感中的应用。此外,得益于 DNA 分子的设计灵活性,通过简单地重新编码相应的识别序列,该构建的生物传感平台实现了适体底物(以卡那霉素为例)和某些金属离子(以汞为例)的灵敏检测,展示了该生物传感平台的良好通用性。

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