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基于多足DNA步行器和主客体技术的可再生电化学生物传感器用于心梗microRNA的高灵敏检测

代志江,单腾腾,李益和,杨建梅,赵焱   

  1. 云南省现代分离分析与物质转化重点实验室,云南师范大学化学化工学院
  • 收稿日期:2025-09-10 修回日期:2025-10-03 网络首发:2025-10-22 发布日期:2025-10-22
  • 通讯作者: 杨建梅 E-mail:yangatynnu@163.com
  • 基金资助:
    国家自然科学基金项目(批准号:22364023)、云南省基础研究计划-面上项目(批准号:202301AT070074)和云南师范大学博士科研启动项目(批准号:2020ZB009)

Regenerable Electrochemical Biosensor Based on Multi-legged DNA Walker and Host-Guest Chemistry for Highly Sensitive Detection of Myocardial Infarction-Related microRNA

DAI Zhijiang,SHAN Tengteng,LI Yihe,YANG Jianmei,ZHAO Yan   

  1. Yunnan Key Laboratory of Modern Separation Analysis and Substance Transformation, College of Chemistry and Chemical Engineering, Yunnan Normal University
  • Received:2025-09-10 Revised:2025-10-03 Online First:2025-10-22 Published:2025-10-22
  • Contact: Jian-Mei YANG E-mail:yangatynnu@163.com
  • Supported by:
    Supported by the National Natural Science Foundation of China (No. 22364023), the Yunnan Fundamental Research Projects, China (No. 202301AT070074), and the PhD Scientific Research Foundation of Yunnan Normal University, China (No. 2020ZB009)

摘要: 本文基于多足DNA步行器和主客体技术,构建了高灵敏检测miRNA-133a-5p的可再生电化学生物传感器。在电极表面修饰还原氧化石墨烯-金纳米颗粒复合材料(rGO@AuNPs)以固定大量的β-环糊精(β-CD),构建可再生传感界面。存在miRNA-133a-5p时,其触发三个发夹DNA探针自组装形成三足DNA步行器,同时置换出miRNA-133a-5p,使其循环参与反应,最终产生大量步行器。步行器高效剪切信号探针,释放出大量二茂铁(Fc)标记的单链DNA片段。这些片段通过主客体作用被电极表面的β-CD捕获,产生电流信号,实现对miRNA-133a-5p的高灵敏检测。由于目标物循环参与反应和三足DNA步行器的高效剪切效率,使传感器的检测限达19.7 fmol/L。同时利用电化学可控调节Fc与β-CD间的主客体作用,使传感器实现6次再生循环利用。本文的研究工作为心梗诊断提供了新平台,也为电化学生物传感器的再生利用提供了有效策略。

关键词: 电化学生物传感器, 急性心肌梗死, DNA步行器, miRNA-133a-5p, 可再生

Abstract: A highly sensitive and regenerable electrochemical biosensor was developed for detecting microRNA-133a-5p (miRNA-133a-5p) by integrating multi-legged DNA walker with host-guest recognition. The sensor featured a regenerable interface constructed by modifying the electrode surface with reduced graphene oxide-gold nanoparticle composites (rGO@AuNPs) and immobilizing abundant β-cyclodextrin (β-CD). Upon introduction of miRNA-133a-5p, the target triggered the self-assembly of three hairpin DNA probes into a three-legged DNA walker. Crucially, miRNA-133a-5p was displaced during this process, enabling its cyclic reuse and subsequent amplification of walker generation. The resulting walkers efficiently cleaved signal probes, yielding numerous ferrocene (Fc)-labeled single-stranded DNA fragments. These fragments were captured by β-CD on the electrode surface via host-guest interactions, generating measurable current signals for ultrasensitive miRNA-133a-5p detection. Benefiting from target recycling amplification and the high cleavage efficiency of the three-legged DNA walker, the sensor achieved a remarkably low detection limit of 19.7 fmol/L. Furthermore, electrochemical regulation of the host-guest interaction between Fc and β-CD facilitated six regeneration cycles. This work establishes a novel platform for myocardial infarction diagnosis and proposes an effective strategy for designing regenerable electrochemical biosensors.

Key words: Electrochemical biosensors; Acute myocardial infarction, DNA walker, miRNA-133a-5p, Regenerable

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