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适体-环 DNA 纳米花识别与多色荧光碳量子点标记系统用于多靶活细胞成像。

Aptamer-Loop DNA Nanoflower Recognition and Multicolor Fluorescent Carbon Quantum Dots Labeling System for Multitarget Living Cell Imaging.

机构信息

College of Biomedical Engineering, Taiyuan University of Technology, 209 University Street, Jinzhong, Shanxi 030600, People's Republic of China.

College of Ecology, Taiyuan University of Technology, 79 West Street Yingze, Taiyuan, Shanxi 030024, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2024 Aug 28;16(34):45327-45336. doi: 10.1021/acsami.4c09358. Epub 2024 Aug 20.

DOI:10.1021/acsami.4c09358
PMID:39161311
Abstract

Visualization of multiple targets in living cells is important for understanding complex biological processes, but it still faces difficulties, such as complex operation, difficulty in multiplexing, and expensive equipment. Here, we developed a nanoplatform integrating a nucleic acid aptamer and DNA nanotechnology for living cell imaging. Aptamer-based recognition probes (RPs) were synthesized through rolling circle amplification, which were further self-assembled into DNA nanoflowers encapsulated by an aptamer loop. The signal probes (SPs) were obtained by conjugation of multicolor emission carbon quantum dots with oligonucleotides complementary to RPs. Through base pairing, RPs and SPs were hybridized to generate aptamer sgc8-, AS1411-, and Apt-based imaging systems. They were used for individual/simultaneous imaging of cellular membrane protein PTK7, nucleolin, and adenosine triphosphate (ATP) molecules. Fluorescence imaging and intensity analysis showed that the living cell imaging system can not only specifically recognize and efficiently bind their respective targets but also provide a 5-10-fold signal amplification. Cell-cycle-dependent distribution of nucleolin and concentration-dependent fluorescence intensity of ATP demonstrated the utility of the system for tracking changes in cellular status. Overall, this system shows the potential to be a simple, low-cost, highly selective, and sensitive living cell imaging platform.

摘要

活细胞中多靶点的可视化对于理解复杂的生物过程非常重要,但它仍然面临着一些困难,例如操作复杂、多重检测困难以及设备昂贵。在这里,我们开发了一种整合核酸适体和 DNA 纳米技术的纳米平台,用于活细胞成像。基于适体的识别探针 (RP) 通过滚环扩增合成,然后进一步自组装成由适体环包裹的 DNA 纳米花。信号探针 (SP) 通过与与 RP 互补的寡核苷酸偶联多色发射碳量子点获得。通过碱基配对,RP 和 SP 杂交生成适体 sgc8、AS1411 和 Apt 成像系统。它们用于单独/同时对细胞膜蛋白 PTK7、核仁素和三磷酸腺苷 (ATP) 分子进行成像。荧光成像和强度分析表明,该活细胞成像系统不仅可以特异性识别和有效结合各自的靶标,还可以提供 5-10 倍的信号放大。核仁素的细胞周期依赖性分布和 ATP 的荧光强度浓度依赖性表明该系统可用于跟踪细胞状态的变化。总的来说,该系统具有成为一种简单、低成本、高选择性和高灵敏度的活细胞成像平台的潜力。

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