Fangfang Yang , Xiaolin Zhang , Shuang Li , Xiaoxiao Yu , Shufeng Liu
{"title":"基于目标刺激释放氧化还原报告物及其催化氧化还原循环的无固定化和无标记电化学 DNA 生物传感技术","authors":"Fangfang Yang , Xiaolin Zhang , Shuang Li , Xiaoxiao Yu , Shufeng Liu","doi":"10.1016/j.bioelechem.2024.108727","DOIUrl":null,"url":null,"abstract":"<div><p>Herein, we demonstrate a simple, homogenous and label-free electrochemical biosensing system for sensitive nucleic acid detection based on target-responsive porous materials and nuclease-triggered target recycling amplification. The Fe(CN)<sub>6</sub><sup>3−</sup> reporter was firstly sealed into the pores of Fe<sub>3</sub>O<sub>4</sub> nanoparticles by probe DNA. Target DNA recognition triggered the controllable release of Fe(CN)<sub>6</sub><sup>3−</sup> for the redox reaction with the electron mediator of methylene blue enriched in the dodecanethiol assembled electrode and thereby generating electrochemical signal. The exonuclease III (Exo III)-assisted target recycling and the catalytic redox recycling between Fe(CN)<sub>6</sub><sup>3−</sup> and methylene blue contributed for the enhanced signal response toward target recognition. The low detection limit toward target was obtained as 478 fM and 1.6 pM, respectively, by square wave voltammetry and cyclic voltammetry methods. It also possessed a well-discrimination ability toward mismatched strands and high tolerance to complex sample matrix. The coupling of bio-gated porous nanoparticles, nuclease-assisted target amplification and catalytic redox recycling afforded the sensing system with well-controllable signal responses, sensitive and selective DNA detection, and good stability, reusability and reproducibility. It thus opens a new avenue toward the development of simple but sensitive electrochemical biosensing platform.</p></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"158 ","pages":"Article 108727"},"PeriodicalIF":4.8000,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Immobilization-free and label-free electrochemical DNA biosensing based on target-stimulated release of redox reporter and its catalytic redox recycling\",\"authors\":\"Fangfang Yang , Xiaolin Zhang , Shuang Li , Xiaoxiao Yu , Shufeng Liu\",\"doi\":\"10.1016/j.bioelechem.2024.108727\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Herein, we demonstrate a simple, homogenous and label-free electrochemical biosensing system for sensitive nucleic acid detection based on target-responsive porous materials and nuclease-triggered target recycling amplification. The Fe(CN)<sub>6</sub><sup>3−</sup> reporter was firstly sealed into the pores of Fe<sub>3</sub>O<sub>4</sub> nanoparticles by probe DNA. Target DNA recognition triggered the controllable release of Fe(CN)<sub>6</sub><sup>3−</sup> for the redox reaction with the electron mediator of methylene blue enriched in the dodecanethiol assembled electrode and thereby generating electrochemical signal. The exonuclease III (Exo III)-assisted target recycling and the catalytic redox recycling between Fe(CN)<sub>6</sub><sup>3−</sup> and methylene blue contributed for the enhanced signal response toward target recognition. The low detection limit toward target was obtained as 478 fM and 1.6 pM, respectively, by square wave voltammetry and cyclic voltammetry methods. It also possessed a well-discrimination ability toward mismatched strands and high tolerance to complex sample matrix. The coupling of bio-gated porous nanoparticles, nuclease-assisted target amplification and catalytic redox recycling afforded the sensing system with well-controllable signal responses, sensitive and selective DNA detection, and good stability, reusability and reproducibility. 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引用次数: 0
摘要
在此,我们展示了一种基于靶响应多孔材料和核酸酶触发靶循环扩增的简单、均质和无标记的电化学生物传感系统,用于灵敏地检测核酸。首先,探针 DNA 将 Fe(CN)63- 报告封入 Fe3O4 纳米粒子的孔隙中。目标 DNA 识别触发了 Fe(CN)63- 的可控释放,与十二硫醇组装电极中富含的电子介质亚甲基蓝发生氧化还原反应,从而产生电化学信号。外切酶 III(Exo III)辅助的目标再循环以及 Fe(CN)63- 和亚甲基蓝之间的催化氧化还原再循环有助于增强对目标识别的信号响应。通过方波伏安法和循环伏安法,对目标物的检测限分别为 478 fM 和 1.6 pM。此外,它还具有对不匹配链的良好分辨能力和对复杂样品基质的高耐受性。生物门控多孔纳米粒子、核酸酶辅助靶标扩增和催化氧化还原再循环的耦合使该传感系统具有良好的信号响应可控性、灵敏度和 DNA 检测选择性,以及良好的稳定性、可重复使用性和可重复性。因此,它为开发简单而灵敏的电化学生物传感平台开辟了一条新途径。
Immobilization-free and label-free electrochemical DNA biosensing based on target-stimulated release of redox reporter and its catalytic redox recycling
Herein, we demonstrate a simple, homogenous and label-free electrochemical biosensing system for sensitive nucleic acid detection based on target-responsive porous materials and nuclease-triggered target recycling amplification. The Fe(CN)63− reporter was firstly sealed into the pores of Fe3O4 nanoparticles by probe DNA. Target DNA recognition triggered the controllable release of Fe(CN)63− for the redox reaction with the electron mediator of methylene blue enriched in the dodecanethiol assembled electrode and thereby generating electrochemical signal. The exonuclease III (Exo III)-assisted target recycling and the catalytic redox recycling between Fe(CN)63− and methylene blue contributed for the enhanced signal response toward target recognition. The low detection limit toward target was obtained as 478 fM and 1.6 pM, respectively, by square wave voltammetry and cyclic voltammetry methods. It also possessed a well-discrimination ability toward mismatched strands and high tolerance to complex sample matrix. The coupling of bio-gated porous nanoparticles, nuclease-assisted target amplification and catalytic redox recycling afforded the sensing system with well-controllable signal responses, sensitive and selective DNA detection, and good stability, reusability and reproducibility. It thus opens a new avenue toward the development of simple but sensitive electrochemical biosensing platform.
期刊介绍:
An International Journal Devoted to Electrochemical Aspects of Biology and Biological Aspects of Electrochemistry
Bioelectrochemistry is an international journal devoted to electrochemical principles in biology and biological aspects of electrochemistry. It publishes experimental and theoretical papers dealing with the electrochemical aspects of:
• Electrified interfaces (electric double layers, adsorption, electron transfer, protein electrochemistry, basic principles of biosensors, biosensor interfaces and bio-nanosensor design and construction.
• Electric and magnetic field effects (field-dependent processes, field interactions with molecules, intramolecular field effects, sensory systems for electric and magnetic fields, molecular and cellular mechanisms)
• Bioenergetics and signal transduction (energy conversion, photosynthetic and visual membranes)
• Biomembranes and model membranes (thermodynamics and mechanics, membrane transport, electroporation, fusion and insertion)
• Electrochemical applications in medicine and biotechnology (drug delivery and gene transfer to cells and tissues, iontophoresis, skin electroporation, injury and repair).
• Organization and use of arrays in-vitro and in-vivo, including as part of feedback control.
• Electrochemical interrogation of biofilms as generated by microorganisms and tissue reaction associated with medical implants.