Xiao Chao-Da, Zhong Ming-Qing, Gao Yue, Yang Zheng-Lin, Jia Meng-Hao, Hu Xiao-Hui, Xu Yan, Shen Xiang-Chun
State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmaceutical Sciences, Guizhou Medical University, Guiyang 550025, China.
The Key Laboratory of Optimal Utilization of Natural Medicine Resources, School of Pharmaceutical Sciences, Guizhou Medical University, Guiyang 550025, China.
Int J Mol Sci. 2023 Sep 20;24(18):14344. doi: 10.3390/ijms241814344.
Surface staining has emerged as a rapid technique for applying external stains to trace cellular identities in diverse populations. In this study, we developed a distinctive aptamer with selective binding to cell surface nucleolin (NCL), bypassing cytoplasmic internalization. Conjugation of the aptamer with a FAM group facilitated NCL visualization on live cell surfaces with laser confocal microscopy. To validate the aptamer-NCL interaction, we employed various methods, including the surface plasmon resonance, IHC-based flow cytometry, and electrophoretic mobility shift assay. The G-quadruplex formations created by aptamers were confirmed with a nuclear magnetic resonance and an electrophoretic mobility shift assay utilizing BG4, a G-quadruplex-specific antibody. Furthermore, the aptamer exhibited discriminatory potential in distinguishing between cancerous and normal cells using flow cytometry. Notably, it functioned as a dynamic probe, allowing real-time monitoring of heightened NCL expression triggered by a respiratory syncytial virus (RSV) on normal cell surfaces. This effect was subsequently counteracted with dsRNA transfection and suppressed the NCL expression; thus, emphasizing the dynamic attributes of the probe. These collective findings highlight the robust versatility of our aptamer as a powerful tool for imaging cell surfaces, holding promising implications for cancer cell identification and the detection of RSV infections.
表面染色已成为一种快速技术,可用于施加外部染料以追踪不同群体中的细胞身份。在本研究中,我们开发了一种独特的适体,它能选择性结合细胞表面核仁素(NCL),避免其内化进入细胞质。将该适体与FAM基团偶联,便于通过激光共聚焦显微镜观察活细胞表面的NCL。为了验证适体与NCL的相互作用,我们采用了多种方法,包括表面等离子体共振、基于免疫组化的流式细胞术和电泳迁移率变动分析。利用BG4(一种G-四链体特异性抗体)通过核磁共振和电泳迁移率变动分析证实了适体形成的G-四链体结构。此外,该适体在使用流式细胞术区分癌细胞和正常细胞方面具有鉴别潜力。值得注意的是,它作为一种动态探针,能够实时监测呼吸道合胞病毒(RSV)在正常细胞表面引发的NCL表达升高。随后,这种效应被双链RNA转染抵消,并抑制了NCL表达;因此,强调了该探针的动态特性。这些共同发现突出了我们的适体作为一种强大的细胞表面成像工具的强大通用性,对癌细胞识别和RSV感染检测具有潜在的应用前景。