化学
生物物理学
极性(国际关系)
溶剂变色
尼罗河红
荧光
纳米技术
显微镜
多路复用
小泡
荧光寿命成像显微镜
分子成像
纳米医学
细胞外小泡
荧光显微镜
微流控
表征(材料科学)
胞外囊泡
纳米尺度
光学成像
微泡
脂质双层
光谱成像
分子生物物理学
材料科学
纳米颗粒
膜
原子力显微镜
免疫金标记
光学镊子
荧光标记
药物输送
高光谱成像
作者
Stijn van Veen,Marije E. Kuipers,Esther Nolte-’t Hoen,Lorenzo Albertazzi
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-01-21
标识
DOI:10.1021/acs.nanolett.5c03118
摘要
Extracellular vesicles (EVs) are attracting growing interest in nanomedicine as nature's own nanocarriers. EV characterization remains challenging, due to complexity and heterogeneity. As such, there is a growing need for experimental techniques that can probe with molecular specificity at the single-particle level. We present a fluidic and super-resolution imaging platform that employs spectral point accumulation for imaging in nanoscale topography (sPAINT) to perform multiplexed imaging of individual EVs derived from prostate cancer (PC3) cells. By combined analysis of the solvatochromic dye Nile Red and fluorescent lectin probes, we can map glycosylation patterns and membrane polarity at the single-particle level, two rather unexplored properties of EVs. Our results reveal pronounced inter- and intraparticle heterogeneity, with polarity signatures consistent with ordered lipid domains. This multiplexed single-molecule imaging strategy enables truly multiparametric EV analysis, allowing the identification of subpopulations that remain indistinguishable in bulk or single-marker approaches.
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