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用于活细胞中miRNA的灵敏传感和精确定位成像的双功能MXene量子点包覆双金属普鲁士蓝类似物

Bifunctional MXene quantum dots-coated bimetallic Prussian blue analogues for sensitive sensing and accurate localization imaging of miRNAs in living cells.

作者信息

You Qiannan, Wang Panyong, Zhu Tongtong, Jia Zixuan, Chang Zhimin, Li Li, Dong Wen-Fei

机构信息

Department of Biomaterials and Stem Cells, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Science, Suzhou, 215163, PR China.

School of Biomedical Engineering (Suzhou), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230026, PR China.

出版信息

Mater Today Bio. 2025 Apr 15;32:101747. doi: 10.1016/j.mtbio.2025.101747. eCollection 2025 Jun.

DOI:10.1016/j.mtbio.2025.101747
PMID:40290880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12032912/
Abstract

MicroRNAs (miRNAs) are involved in multiple cellular processes and play a critical role in clinical diagnosis. In-situ spatiotemporal imaging of miRNAs in living cells is tightly linked to the carcinogenesis and development of malignant tumors. Herein, we proposed a bifunctional nanosystem-based MXene quantum dots-coated bimetallic Prussian blue analogues (Co-Mn PBA@MQDs) to execute in-vitro sensing and intracellular imaging of miRNA in living cells. The 3D nanostructures of Co-Mn PBAs were regulated to slow down the coordination reaction rate by controlling the diffusion of metal clusters and ligand precursors, thereby anchoring MQDs as the carriers of DNA probes. The resulting Co-Mn PBA@MQDs nanoparticles with miRNA recognition ability exhibit excellent electrocatalytic and photoluminescence properties for target miRNA analysis. It reached miRNA detection limit of 0.37 fM (S/N = 3) with a wide linear range of 1 fM to 1 nM, and allowed distinguish family members without additional complex modifications. Meanwhile, DNA probe adsorbed on Co-Mn PBA@MQDs can provide delivery capacity for intracellular miRNA location, resulting in the in-situ monitoring and imaging of miRNA with deregulated expression levels in cancer cells. With these advantages, the developed strategy provides a paradigm for the rational design of the miRNA analysis system, which is expected to be widely applied to disease diagnosis and further theragnostic fields.

摘要

微小RNA(miRNA)参与多种细胞过程,在临床诊断中发挥关键作用。活细胞中miRNA的原位时空成像与恶性肿瘤的发生发展密切相关。在此,我们提出了一种基于双功能纳米系统的MXene量子点包覆双金属普鲁士蓝类似物(Co-Mn PBA@MQDs),用于在活细胞中进行miRNA的体外传感和细胞内成像。通过控制金属簇和配体前体的扩散来调节Co-Mn PBAs的三维纳米结构,以减缓配位反应速率,从而将MQDs锚定作为DNA探针的载体。所得具有miRNA识别能力的Co-Mn PBA@MQDs纳米颗粒对目标miRNA分析表现出优异的电催化和光致发光特性。它实现了0.37 fM的miRNA检测限(S/N = 3),线性范围宽达1 fM至1 nM,且无需额外复杂修饰就能区分家族成员。同时,吸附在Co-Mn PBA@MQDs上的DNA探针可为细胞内miRNA定位提供递送能力,从而对癌细胞中表达水平失调的miRNA进行原位监测和成像。凭借这些优势,所开发的策略为miRNA分析系统的合理设计提供了范例,有望广泛应用于疾病诊断及进一步的诊疗领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/a2f4aa654a9a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/acb03935c434/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/4ea370e38fab/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/3b443dbc567b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/584f128b6342/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/35bfa3432625/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/ce7e7a1cb1a0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/a2f4aa654a9a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/acb03935c434/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/4ea370e38fab/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/3b443dbc567b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/584f128b6342/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/35bfa3432625/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/ce7e7a1cb1a0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168c/12032912/a2f4aa654a9a/gr5.jpg

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