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DNA 酶驱动的双足 DNA walker 引发杂交银纳米粒子探针用于淀粉样β寡聚体的电化学检测。

DNAzyme-driven bipedal DNA walker triggered to hybridize silver nanoparticle probes for electrochemical detection of amyloid-β oligomer.

机构信息

The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, China.

School of Pharmacy, Xuzhou Medical University, 221004, Xuzhou, China.

出版信息

Anal Chim Acta. 2023 Mar 15;1246:340889. doi: 10.1016/j.aca.2023.340889. Epub 2023 Jan 25.

DOI:10.1016/j.aca.2023.340889
PMID:36764775
Abstract

Amyloid-β oligomer has been considered as a promising molecular biomarker for the diagnosis of Alzheimer's disease due to their significant neural synapse toxicity. Therefore, it is essential to create an easy approach for the selective detection of Amyloid-β oligomer that has high sensitivity and cheap cost. In this work, we developed an innovative enzyme-free electrochemical aptasensor based on the DNAzyme-driven DNA bipedal walker tactics for sensing Amyloid-β oligomer. Bipedal DNA walkers demonstrate a wider walking region, better walking kinetics, and higher amplification effectiveness than typical DNA walkers. The Mg-dependent DNAzyme drove the DNA walker, and the binding-induced DNA walker can sequentially shear MBs and form MB fragment structure. Finally, the detection probes modified AgNPs hybridized with the MB fragment structure, resulting in the multiplication of AgNPs on the electrode surface. Electrochemical stripping of AgNPs was used to test the performance of the obtained electrochemical sensor. In particular, a low detection limit of 5.94 fM and a wide linear range of 0.01 pM-0.1 nM were attained. The detection of Amyloid-β oligomer in human serum was then carried out using this bipedal DNA walker biosensor, which shown good selectivity and outstanding reproducibility, indicating its usefulness in bioanalysis.

摘要

淀粉样β寡聚体由于其显著的神经突触毒性,已被认为是阿尔茨海默病诊断有前途的分子生物标志物。因此,开发一种简单的方法来选择性检测淀粉样β寡聚体具有高灵敏度和低成本是至关重要的。在这项工作中,我们开发了一种基于 DNA 酶驱动 DNA 双足步行策略的无酶电化学适体传感器,用于检测淀粉样β寡聚体。双足 DNA walker 比典型的 DNA walker 具有更宽的行走区域、更好的行走动力学和更高的放大效率。Mg 依赖性 DNA 酶驱动 DNA walker,而结合诱导的 DNA walker 可以依次剪切 MBs 并形成 MB 片段结构。最后,检测探针修饰的 AgNPs 与 MB 片段结构杂交,导致 AgNPs 在电极表面的增殖。AgNPs 的电化学剥离被用于测试所获得的电化学传感器的性能。特别是,获得了 5.94 fM 的低检测限和 0.01 pM-0.1 nM 的宽线性范围。然后使用这种双足 DNA walker 生物传感器进行了人血清中淀粉样β寡聚体的检测,结果显示出良好的选择性和出色的重现性,表明其在生物分析中的有用性。

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