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无标记和超灵敏的 DNA 阻抗传感器,具有酶和电双重扩增。

A label-free and ultrasensitive DNA impedimetric sensor with enzymatic and electrical dual-amplification.

机构信息

State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Electronic Science, Xiamen University, Xiamen 361005, P. R. China.

出版信息

Analyst. 2019 Jul 8;144(14):4175-4179. doi: 10.1039/c9an00682f.

Abstract

In this work, we report a facile, sensitive, selective, and reproducible DNA impedimetric sensor device. We demonstrate that, combined with exonuclease III, the easily prepared electrochemically reduced graphene oxide (rGO) could be a desirable platform to amplify signals in electrochemical impedance spectroscopy for ultrasensitive DNA detection. Guided by enzyme assisted target recycling, efficient interfacial tuning can be obtained, from the situation with high impedance caused by single-stranded DNA probes directly adsorbed onto rGO to the one with low impedance due to the continuous desorption of target-probe DNA hybrids and the consequent digestion of DNA probes. Just a few DNA targets can specifically trigger the enzymatic digestion of a large number of DNA probes. It is the excellent electrical conductivity of rGO that further enlarges the changes of electron transfer resistance after the removal of DNA probes. As a result of synergistically combining both enzymatic and electrical amplification, the enlarged changes of impedimetric signals can be measured to sensitively report DNA targets. The specificity has been guaranteed by the intrinsic recognition of hybrids through both rGO and exonuclease III. A limit of detection as low as 10 aM target DNA in the matrix of cell culture medium, as well as a wide linear range and good discrimination of mismatched sequences even at the one-base level, suggests its great application prospect in biosensing and biomedical analysis. It also has other advantages including easy operation, low cost, and convenient regeneration, with more competitive performance in developing impedimetric biosensors.

摘要

在这项工作中,我们报道了一种简便、灵敏、选择性好且重现性好的 DNA 阻抗传感器。我们证明,与外切酶 III 结合使用,易于制备的电化学还原氧化石墨烯(rGO)可以成为电化学阻抗谱中用于超灵敏 DNA 检测的信号放大的理想平台。在酶辅助靶标循环的指导下,可以实现有效的界面调谐,从单链 DNA 探针直接吸附在 rGO 上导致高阻抗的情况转变为由于目标-探针 DNA 杂交物的连续解吸和随后的 DNA 探针消化导致的低阻抗情况。只需少量的 DNA 靶标就能特异性地触发大量 DNA 探针的酶促消化。正是 rGO 的优异导电性进一步放大了 DNA 探针去除后电子转移电阻的变化。通过酶和电的协同放大,放大后的阻抗信号变化可以被测量以灵敏地报告 DNA 靶标。通过 rGO 和外切酶 III 对杂交物的固有识别保证了特异性。在细胞培养基基质中,检测限低至 10 aM 的目标 DNA,以及即使在单个碱基水平上也能很好地区分错配序列的宽线性范围和良好的辨别能力,表明其在生物传感和生物医学分析中有很大的应用前景。它还具有其他优点,包括操作简单、成本低、易于再生,在开发阻抗生物传感器方面具有更具竞争力的性能。

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