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新型二维 DNA-纳米探针介导的无酶靶标循环扩增用于超灵敏电化学检测 microRNA。

Novel 2D-DNA-Nanoprobe-Mediated Enzyme-Free-Target-Recycling Amplification for the Ultrasensitive Electrochemical Detection of MicroRNA.

机构信息

Key Laboratory of Luminescence and Real-Time Analytical Chemistry, Ministry of Education, College of Chemistry and Chemical Engineering , Southwest University , Chongqing 400715 , PR China.

出版信息

Anal Chem. 2018 Aug 7;90(15):9538-9544. doi: 10.1021/acs.analchem.8b02251. Epub 2018 Jul 19.

Abstract

In this work, on the basis of a new 2D DNA nanoprobe (DNP) and an enzyme-free-target-recycling amplification, an electrochemical biosensor is developed for the ultrasensitive detection of microRNA-21 (miRNA-21). Herein, two ferrocene-labeled bipedal DNPs, which show small steric hindrance and strong stability, are prepared on the basis of the mechanism of the proximity-ligation assay (PLA), improving the space utilization. In the presence of the target, miRNA-21, and a hairpin DNA strand, the DNP will collapse, and then two ferrocene-labeled DNA strands and the miRNA-21 will be simultaneously released from the electrode surface through toehold-mediated strand-displacement reactions (TSDRs), leading to a decrease in the electrochemical signal and realization of enzyme-free target recycling. As a result, the one input target, miRNA-21, could release 2 N ferrocene-labeled DNA strands, achieving a dramatic decrease in the electrochemical signal. Combining DNPs and enzyme-free target recycling, this proposed biosensor showed a linear dependence with miRNA-21 concentration, ranging from 1.0 fM to 10 nM with a detection limit of 0.31 fM. In addition, it is worth mentioning that this biosensor can be regenerated through incubating with three assistant-DNA strands, realizing the reuse of raw materials. Surprisingly, the elaborated biosensor provides a novel strategy for building controllable DNA nanoprobes for the sensitive detection of various biomarkers.

摘要

在这项工作中,基于一种新型的 2D DNA 纳米探针(DNP)和无酶靶标循环扩增,开发了一种电化学生物传感器,用于超灵敏检测 microRNA-21(miRNA-21)。在此基础上,基于接近连接分析(PLA)的机制,制备了两种具有较小空间位阻和较强稳定性的双足 Ferrocene 标记的双足 DNA 探针,提高了空间利用率。在存在靶标、miRNA-21 和发夹 DNA 链的情况下,DNP 会坍塌,然后通过钉位介导的链置换反应(TSDR),两个 Ferrocene 标记的 DNA 链和 miRNA-21 同时从电极表面释放,导致电化学信号降低并实现无酶靶标循环。因此,一个输入的靶标 miRNA-21 可以释放 2N 的 Ferrocene 标记的 DNA 链,从而导致电化学信号急剧下降。结合 DNP 和无酶靶标循环,该生物传感器在 miRNA-21 浓度范围内表现出线性关系,从 1.0 fM 到 10 nM,检测限为 0.31 fM。此外,值得一提的是,该生物传感器可以通过孵育三种辅助 DNA 链进行再生,实现原材料的再利用。令人惊讶的是,精心设计的生物传感器为构建用于敏感检测各种生物标志物的可控 DNA 纳米探针提供了一种新策略。

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