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基于近邻杂交引发的锚定单足 DNA 分子马达用于扩增电流型生物传感检测核酸和蛋白质

An anchored monopodial DNA walker triggered by proximity hybridization for amplified amperometric biosensing of nucleic acid and protein.

机构信息

Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Tropical Medicine and Laboratory Medicine, Hainan Medical University, Haikou, 571199, PR China; Affiliated Hospital of Southwest Medical University, Luzhou, 646000, PR China.

Affiliated Hospital of Southwest Medical University, Luzhou, 646000, PR China.

出版信息

Anal Chim Acta. 2020 Apr 22;1107:48-54. doi: 10.1016/j.aca.2020.02.013. Epub 2020 Feb 7.

Abstract

This work designed an anchored monopodial DNA walker to amplify amperometric biosensing signal for sensitive detection of nucleic acid and protein. The biosensing surface was constructed by self-assembling hairpin DNA1 (H1) and small amount of P1-W (probe DNA1 hybridized with walking DNA) on a gold electrode. In the presence of target molecule, the walker could be triggered by the surface proximity hybridization product of P1, target and P2 to induce the cyclic hybridization of H1 with ferrocene modified hairpin DNA2 (H2-Fc), which took electroactive Fc to the electrode surface for amplified amperometric detection of the target. By linking P1 and P2 with dual specific DNA strands, aptamers or antibodies to recognize the target for proximity hybridization of P1 and P2, the walker amplified amperometric strategy could be used for highly sensitive biosensing of different targets. Using DNA and thrombin as the target models, the proposed biosensing methods achieved the linear range from 0.2 pM to 2 nM with a detection limit of 0.11 pM and 1.0 pM to 10 nM with a detection limit of 0.61 pM, respectively. The specific recognition process endowed the strategy with high selectivity and potential applications.

摘要

本工作设计了一种锚定的单足 DNA walker,用于放大安培生物传感信号,以实现对核酸和蛋白质的灵敏检测。生物传感表面通过自组装发夹 DNA1(H1)和少量与行走 DNA 杂交的 P1-W(探针 DNA1)在金电极上构建。在存在靶分子的情况下,walker 可以被 P1、靶和 P2 的表面近邻杂交产物触发,诱导 H1 与二茂铁修饰的发夹 DNA2(H2-Fc)的循环杂交,将电化学活性的 Fc 带到电极表面,用于对靶的放大安培检测。通过将 P1 和 P2 与双特异性 DNA 链、适体或抗体连接,以识别靶分子进行 P1 和 P2 的近邻杂交,walker 放大安培策略可用于不同靶标的高灵敏度生物传感。使用 DNA 和凝血酶作为靶标模型,所提出的生物传感方法分别实现了从 0.2 pM 到 2 nM 的线性范围,检测限为 0.11 pM,以及从 1.0 pM 到 10 nM 的线性范围,检测限为 0.61 pM。特定的识别过程赋予了该策略高选择性和潜在的应用。

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