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

适体 核仁素 荧光 纳米技术 生物物理学 荧光寿命成像显微镜 量子点 滚动圆复制 费斯特共振能量转移 DNA 活体细胞成像 材料科学 寡核苷酸 细胞 化学 细胞生物学 生物 分子生物学 生物化学 DNA复制 物理 量子力学 细胞质 核仁
作者
Xilin Guo,Baohua Tian,Xinxin Li,Lei Yu,Mingyuan Sun,Qiang Miao,Hao Li,Ri-Sheng Ma,Haixia Liang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (34): 45327-45336 被引量:9
标识
DOI:10.1021/acsami.4c09358
摘要

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.
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