用于高保真microRNA成像和临床液体活检的自组装DNA纳米球驱动的无约束自循环放大器。

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Talanta Pub Date : 2027-02-01 Epub Date: 2026-08-07 DOI:10.1016/j.talanta.2026.130416
Jing Jiang, Guohai Lin, Hengxin Yu, Liqun Chen, Huo Xu
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引用次数: 0

摘要

开发可预测和热力学稳定的DNA纳米机器对复杂生物基质中细胞内microrna (mirna)的监测仍然具有挑战性。在本研究中,提出了一种利用无限制协同配置的荧光生物传感器来精确检测miR-21。为了减轻均相催化发夹组装(CHA)的热力学限制,放大组件在空间上进行了划分。CHA是一个无约束的分子扩散引起背景泄漏的过程。传感平台采用刚性DNA纳米球(NP),通过三个回文序列的退火组装,作为一个空间阻碍支架,严格限制发夹探针1 (HP1)。靶miR-21开启锚定的HP1,随后招募可自由扩散的辅助探针(HP2和HP3),形成局部的y形复合物。该反应产生替代miR-21序列,该序列分离并解锁相邻的HP1探针,建立颗粒间化学通信网络。通过将纳米尺度的空间约束与这种传播的催化级联相结合,所提出的无约束自循环放大器(CF-SCA)在保持快速传质的同时抑制背景泄漏,产生100 pM的检测极限。此外,致密的3D纳米支架提供了核酸酶抗性。在脂质体介导的细胞递送之后,这种不受限制的机制抵消了大分子拥挤,促进了miR-21在活癌细胞中的原位动态成像。通过对来自多个癌症队列的临床血清样本进行分层评估,CF-SCA纳米平台为临床诊断和液体活检应用提供了一种无酶工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self-assembled DNA nanosphere-powered confined-free self-circulating amplifier for high-fidelity microRNA imaging and clinical liquid biopsy.

The development of predictable and thermodynamically stable DNA nanomachines remains challenging for the monitoring of intracellular microRNAs (miRNAs) in complex biological matrices. In this study, a fluorescent biosensor utilizing a confined-free synergistic configuration is presented for the precise detection of miR-21. To mitigate the thermodynamic limitations of homogeneous catalytic hairpin assembly (CHA), a process in which unconstrained molecular diffusion induces background leakage, the amplification components were spatially partitioned. The sensing platform incorporates a rigid DNA nanosphere (NP), assembled via the annealing of three palindromic sequences, which serves as a sterically hindered scaffold to strictly confine hairpin probe 1 (HP1). Target miR-21 initiates the opening of the anchored HP1, subsequently recruiting freely diffusible auxiliary probes (HP2 and HP3) to form a localized Y-shaped complex. This reaction generates a surrogate miR-21 sequence that detaches and unlocks adjacent HP1 probes, establishing an inter-particle chemical communication network. By integrating nanoscale spatial confinement with this propagated catalytic cascade, the proposed confined-free self-circulating amplifier (CF-SCA) suppresses background leakage while maintaining rapid mass transfer, yielding a limit of detection of 100 pM. Additionally, the dense 3D nanoscaffold provides nuclease resistance. Following liposome-mediated cellular delivery, the confined-free mechanism counteracts macromolecular crowding, facilitating in situ dynamic imaging of miR-21 in living cancer cells. Evaluated through the stratification of clinical serum samples from multiple cancer cohorts, the CF-SCA nanoplatform offers an enzyme-free tool for clinical diagnostics and liquid biopsy applications.

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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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