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一种基于exonuclease 辅助扩增的电化学适体传感器,用于凝血酶的“信号开/关”策略耦合。

An exonuclease-assisted amplification electrochemical aptasensor of thrombin coupling "signal on/off" strategy.

机构信息

Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules & College of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062, PR China.

Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules & College of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062, PR China.

出版信息

Anal Chim Acta. 2015 Feb 20;860:70-6. doi: 10.1016/j.aca.2014.12.027. Epub 2014 Dec 17.

Abstract

In this work, a dual-signaling electrochemical aptasensor based on exonuclease-catalyzed target recycling was developed for thrombin detection. The proposed aptasensor coupled "signal-on" and "signal-off" strategies. As to the construction of the aptasensor, ferrocene (Fc) labeled thrombin binding aptamer (TBA) could perfectly hybridize with the methylene blue (MB) modified thiolated capture DNA to form double-stranded structure, hence emerged two different electrochemical signals. In the presence of thrombin, TBA could form a G-quadruplex structure with thrombin, leading to the dissociation of TBA from the duplex DNA and capture DNA formed hairpin structure. Exonuclease could selectively digest single-stranded TBA in G-quadruplex structure and released thrombin to realize target recycling. As a consequence, the electrochemical signal of MB enhanced significantly, which realized "signal on" strategy, meanwhile, the deoxidization peak current of Fc decreased distinctly, which realized "signal off" strategy. The employment of exonuclease and superposition of two signals significantly improved the sensitivity of the aptasensor. In this way, an aptasensor with high sensitivity, good stability and selectivity for quantitative detection of thrombin was constructed, which exhibited a good linear range from 5 pM to 50 nM with a detection limit of 0.9 pM (defined as S/N=3). In addition, this design strategy could be applied to the detection of other proteins and small molecules.

摘要

在这项工作中,开发了一种基于外切酶催化靶标循环的双重信号电化学适体传感器,用于凝血酶检测。所提出的适体传感器结合了“信号开启”和“信号关闭”策略。在适体传感器的构建中,标记有二茂铁(Fc)的凝血酶结合适体(TBA)可以与亚甲基蓝(MB)修饰的巯基化捕获 DNA 完美杂交,形成双链结构,从而出现两种不同的电化学信号。在存在凝血酶的情况下,TBA 可以与凝血酶形成 G-四链体结构,导致 TBA 从双链 DNA 和捕获 DNA 解离形成发夹结构。外切酶可以选择性地消化 G-四链体结构中的单链 TBA,并释放凝血酶以实现目标循环。因此,MB 的电化学信号显著增强,实现了“信号开启”策略,同时,Fc 的还原峰电流明显降低,实现了“信号关闭”策略。外切酶的使用和两种信号的叠加显著提高了适体传感器的灵敏度。通过这种方式,构建了一种具有高灵敏度、良好稳定性和选择性的适体传感器,用于定量检测凝血酶,其线性范围从 5 pM 到 50 nM,检测限为 0.9 pM(定义为 S/N=3)。此外,这种设计策略可应用于其他蛋白质和小分子的检测。

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