4.7 Article

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

Journal

ANALYTICA CHIMICA ACTA
Volume 1278, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2023.341715

Keywords

Programmable biosensing; Entropy-driven catalytic; Catalytic hairpin assembly; Cascade amplification; Ratiometric biosensor

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In this study, a programmable biosensing platform was developed by ingeniously integrating powerful DNA strand displacement reaction and sensitive electrochemical analysis method. A cascade amplification system based on catalytic hairpin assembly and entropy-driven catalytic was constructed to significantly improve the reaction rate and signal amplification effect. 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 achieve highly sensitive detection of the target. Moreover, the biosensing platform demonstrated good versatility by realizing the sensitive detection of aptamer substrate and certain metal ion simply by recoding the corresponding recognition sequence.
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.

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