利用行走-循环-转换策略进行核苷酸蛋白双模式检测的多空间定位 DNA 沃克耦合共价有机框架。

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Analytical Chemistry Pub Date : 2024-11-19 Epub Date: 2024-11-05 DOI:10.1021/acs.analchem.4c03846
Guanxia Qiu, Yuqi Wang, WanWan Zhang, Ting Bao, Zhen Wu, Xiuhua Zhang, Shengfu Wang, Wei Wen
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引用次数: 0

摘要

DNA 漫步器已成为生物分析领域的有力工具;然而,许多现有方法仍受到反应动力学低和单模检测不准确的限制。本文提出了一种基于多空间定位 DNA 步行器(m-DNA walker)的荧光(FL)和电化学(EC)双模生物传感器,该传感器采用步行-回收-转换策略,将共价有机框架(COF)耦合在一起。具体来说,功能化 COF 不仅是一种三维纳米载体,而且还是行走轨迹的有效淬灭剂。在靶标存在的情况下,被激活的 m-DNA 步行器沿着众多淬灭轨道快速移动,导致 Cy3-H1 被裂解,FL 信号恢复。为了进一步提高检测灵敏度,Cy3-H1 片段的回收过程产生了大量的 S1 和 S2,从而在电极上组装了 DNA-Fe3+ 聚多巴胺网络放大器。引入快速电化学转换,将 DNA-Fe3+-polydopamine 转化为电活性普鲁士蓝,提供显著的电化学信号输出。以核壳蛋白(N-protein)为模型靶标,所设计的生物传感平台产生了 FL/EC 双模式读数,FL 模式的检测限为 65.0 fg/mL,EC 模式的检测限为 2.3 fg/mL,可以消除不同反应途径的干扰,提高检测精度,有望应用于疾病的早期诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multispatially Localized DNA Walker Coupling Covalent Organic Framework for Dual-Mode Detection of Nucleocapsid Protein Using the Walking-Recycling-Conversion Strategy.

Multispatially Localized DNA Walker Coupling Covalent Organic Framework for Dual-Mode Detection of Nucleocapsid Protein Using the Walking-Recycling-Conversion Strategy.

DNA walkers have emerged as a powerful tool in bioanalysis; however, many existing approaches are still restricted by low reaction kinetics and inaccurate single-mode detection. Herein, a fluorescence (FL) and electrochemical (EC) dual-mode biosensor was proposed based on a multispatially localized DNA walker (m-DNA walker) coupling covalent organic framework (COF) using the walking-recycling-conversion strategy. Specifically, the functionalized COF not only served as a three-dimensional nanocarrier but also acted as an effective quencher of the walking tracks. In the presence of the target, the activated m-DNA walker moved fast along the numerous quenching tracks, leading to the cleavage of Cy3-H1 and the recovery of the FL signal. To further improve the detection sensitivity, the Cy3-H1 fragments' recycling process was implemented with the generation of a large amount of S1 and S2, which caused the assembly of DNA-Fe3+-polydopamine network amplifiers on the electrode. The rapid electrochemical conversion was introduced to convert DNA-Fe3+-polydopamine into electroactive Prussian Blue, providing a significant EC signal output. Using nucleocapsid protein (N-protein) as the model target, the designed biosensing platform produced a FL/EC dual-mode readout with the detection limits of 65.0 fg/mL for FL mode and 2.3 fg/mL for EC mode, which could eliminate the interference from different reactive pathways and improve the detection accuracy, holding potential application in early disease diagnosis and treatment.

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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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