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基于引发链置换反应和 DSN 酶辅助扩增的电化学生物传感平台用于双靶标检测。

Electrochemical Biosensing Platform Based on Toehold-Mediated Strand Displacement Reaction and DSN Enzyme-Assisted Amplification for Two-Target Detection.

机构信息

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, P. R. China.

School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China.

出版信息

ACS Appl Mater Interfaces. 2024 Aug 28;16(34):45695-45703. doi: 10.1021/acsami.4c08515. Epub 2024 Aug 19.

Abstract

Simultaneous detection of multiple targets is of great significance for accurate disease diagnosis. Herein, based on duplex-specific nuclease (DSN) assisted signal amplification and the toehold-mediated strand displacement reaction (TSDR), we constructed an electrochemical biosensor with high sensitivity and high specificity for dual-target detection. MiRNA-141 and miRNA-133a were used as the targets, and ferrocene (Fc) and methylene blue (MB) with significant peak potential differentiation were used as the electrochemical signal probes. The elaborately designed hairpin probe H1, which was fixed on the electrode surface, could be hybridized with the target miRNA-141 to perform signal amplification by the DSN-assisted enzyme cleavage cycle; thus, miRNA-141 could be detected by Fc signal changes at 0.41 V. The hairpin H1 can also combine with the MB-labeled signal probe (SP) output from miRNA-133a-induced TSDR, and the detection of miRNA-133a can be realized according to the response signal generated by MB at -0.26 V. The two sensing lines are independent of each other, and there is no mutual interference in the detection process. Therefore, two independent detection lines could be connected in series, and the simultaneous detection of two targets can be achieved on a single electrode. This novel detection strategy provides a new way to simultaneously detect different biomarkers.

摘要

同时检测多个目标对于准确的疾病诊断具有重要意义。在此,我们基于双链特异性核酸酶(DSN)辅助的信号放大和链置换反应(TSDR)构建了一种具有高灵敏度和高特异性的用于双重靶标检测的电化学生物传感器。miRNA-141 和 miRNA-133a 被用作靶标,具有显著峰电位差异的二茂铁(Fc)和亚甲蓝(MB)被用作电化学信号探针。精心设计的发夹探针 H1 固定在电极表面上,与靶标 miRNA-141 杂交,通过 DSN 辅助的酶切割循环进行信号放大;因此,可以通过 Fc 信号在 0.41 V 处的变化来检测 miRNA-141。发夹 H1 还可以与 miRNA-133a 诱导的 TSDR 产生的 MB 标记的信号探针(SP)结合,根据 MB 在 -0.26 V 处产生的响应信号可以实现对 miRNA-133a 的检测。两条传感线相互独立,在检测过程中没有相互干扰。因此,可以将两个独立的检测线串联连接,在单个电极上实现对两个目标的同时检测。这种新颖的检测策略为同时检测不同的生物标志物提供了新途径。

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