菁
化学
荧光
尼罗河红
共焦显微镜
生物物理学
Zeta电位
共焦
荧光显微镜
小泡
两亲性
细胞外
活体细胞成像
膜
光化学
纳米颗粒
纳米技术
生物化学
细胞
有机化学
物理
细胞生物学
数学
生物
材料科学
聚合物
共聚物
量子力学
几何学
作者
Takashi Shimomura,Ryo Seino,Kaori Umezaki,Asako Shimoda,Takatoshi Ezoe,Munetaka Ishiyama,Kazunari Akiyoshi
标识
DOI:10.1021/acs.bioconjchem.1c00068
摘要
PKH dyes, which are currently the most widely used fluorescent probes for extracellular vesicle (EV) labeling, have some limitations. For example, these dyes tend to aggregate, leading to formation of EV-like nanoparticles that can be taken up by cells. Moreover, it has been suggested that PKH dyes trigger an enlargement of EVs because of membrane fusion or intercalation. To overcome these limitations, we developed three novel extracellular vesicular-membrane-binding fluorescent probes-Mem dye-Green, Mem dye-Red, and Mem dye-Deep Red-for monitoring EV uptake into cells. The dyes contain a cyanine group as a fluorescent scaffold and amphiphilic moieties on the cyanine. The three dyes have different photophysical characteristics. To investigate the characteristics of the Mem dyes for EV labeling, we performed nanoparticle tracking, zeta potential measurements, and confocal microscopy. The dyes enable highly sensitive fluorescence imaging of EVs. They can also be used to observe EV dynamics in live cells. The Mem dyes show excellent EV labeling with no aggregation and less particle enlargement.
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