Target-driven cascade amplified assembly of covalent organic frameworks on tetrahedral DNA nanostructure with multiplex recognition domains for ultrasensitive detection of microRNA

IF 6 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Hongying Yang, Yunxia Jin, Hui Qian, Yuqi Wang, Ting Bao, Zhen Wu, Wei Wen, Xiuhua Zhang, Shengfu Wang
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引用次数: 0

Abstract

Background

MicroRNA (miRNA) emerges as important cancer biomarker, accurate detection of miRNA plays an essential role in clinical sample analysis and disease diagnosis. However, it remains challenging to realize highly sensitive detection of low-abundance miRNA. Traditional detection methods including northern blot and real-time PCR have realized quantitative miRNA detection. However, these detection methods are involved in sophisticated operation and expensive instruments. Therefore, the development of novel sensing platform with high sensitivity and specificity for miRNA detection is urgently demanded for disease diagnosis.

Results

In this work, a novel electrochemical biosensor was constructed for miRNA detection based on target-driven cascade amplified assembly of electroactive covalent organic frameworks (COFs) on tetrahedral DNA nanostructure with multiplex recognition domains (m-TDN). COFs were employed as nanocarriers of electroactive prussian blue (PB) molecules by the “freeze-drying-reduction” method without the use of DNA as gatekeeper, which was simple, mild and efficient. The target-triggered catalytic hairpin assembly (CHA) and glutathione reduction could convert low-abundance miRNA into a large amount of Mn2+. Without the addition of exogenous Mn2+, the dynamically-generated Mn2+-powered DNAzyme cleavage process induced abundant PB-COFs probe assembled on the four recognition domains of m-TDN, resulting in significantly signal output. Using miRNA-182-5p as the model target, the proposed electrochemical biosensor achieved ultrasensitive detection of miRNA-182-5p in the range of 10 fM-100 nM with a detection limit of 2.5 fM.

Significance and novelty

Taking advantages of PB-COFs probe as the enhanced signal labels, the integration of CHA, Mn2+-powered DNAzyme and m-TDN amplification strategy significantly improved the sensitivity and specificity of the biosensor. The designed sensing platform was capable of miRNA detection in complex samples, which provided a new idea for biomarker detection, holding promising potential in clinical diagnosis and disease screening.

Abstract Image

在具有多重识别域的四面体 DNA 纳米结构上组装共价有机框架的目标驱动级联放大技术,用于超灵敏微 RNA 检测
背景microRNA(miRNA)已成为重要的癌症生物标志物,准确检测miRNA在临床样本分析和疾病诊断中起着至关重要的作用。然而,实现对低丰度 miRNA 的高灵敏度检测仍具有挑战性。传统的检测方法包括 Northern 印迹和实时 PCR,已实现了 miRNA 的定量检测。然而,这些检测方法操作复杂、仪器昂贵。结果 在这项工作中,我们构建了一种新型的电化学生物传感器,用于检测 miRNA。该传感器是基于靶标驱动的级联放大组装,将电活性共价有机框架(COFs)组装在具有多重识别域(m-TDN)的四面体 DNA 纳米结构上。采用 "冻干-还原 "方法将COFs作为电活性普鲁士蓝(PB)分子的纳米载体,不使用DNA作为守门员,简单、温和、高效。目标触发的催化发夹组装(CHA)和谷胱甘肽还原可以将低丰度的 miRNA 转化为大量的 Mn2+。在不添加外源 Mn2+ 的情况下,动态产生的 Mn2+ 驱动的 DNA 酶裂解过程诱导大量 PB-COFs 探针组装在 m-TDN 的四个识别域上,从而产生显著的信号输出。以 miRNA-182-5p 为模型靶标,所提出的电化学生物传感器实现了对 miRNA-182-5p 的超灵敏检测,检测范围为 10 fM-100 nM,检测限为 2.5 fM。所设计的传感平台能够检测复杂样品中的 miRNA,为生物标记物检测提供了新思路,在临床诊断和疾病筛查中具有广阔的应用前景。
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来源期刊
Analytica Chimica Acta
Analytica Chimica Acta 化学-分析化学
CiteScore
10.40
自引率
6.50%
发文量
1081
审稿时长
38 days
期刊介绍: Analytica Chimica Acta has an open access mirror journal Analytica Chimica Acta: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. Analytica Chimica Acta provides a forum for the rapid publication of original research, and critical, comprehensive reviews dealing with all aspects of fundamental and applied modern analytical chemistry. The journal welcomes the submission of research papers which report studies concerning the development of new and significant analytical methodologies. In determining the suitability of submitted articles for publication, particular scrutiny will be placed on the degree of novelty and impact of the research and the extent to which it adds to the existing body of knowledge in analytical chemistry.
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