化学
共焦
荧光
内化
生物物理学
细胞
细胞膜
罗丹明
膜
细胞外
细胞内
荧光寿命成像显微镜
两亲性
活体细胞成像
内吞作用
纳米技术
生物化学
物理
材料科学
有机化学
生物
共聚物
聚合物
几何学
数学
量子力学
作者
Zixu He,Diankai Liu,He Li,Wenjie Gao,Xiaohua Li,Huimin Ma,Wen Shi
标识
DOI:10.1021/acs.analchem.4c00946
摘要
Confocal fluorescence imaging of fine structures of the cell membrane is important for understanding their biofunctions but is often neglected due to the lack of an effective method. Herein, we develop new amphiphilic rhodamine fluorescent probe RMGs in combination with basal imaging for this purpose. The probes show high signal-to-noise ratio and brightness and low internalization rate, making them suitable for imaging the fine substructures of the cell membrane. Using the representative probe RMG3, we not only observed the cell pseudopodia and intercellular nanotubes but also monitored the formation of migrasomes in real time. More importantly, in-depth imaging studies on more cell lines revealed for the first time that hepatocellular carcinoma cells secreted much more adherent extracellular vesicles than other cell lines, which might serve as a potential indicator of liver cells. We believe that RMGs may be useful for investigating the fine structures of the cell membrane.
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