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Sizing subcellular organelles and nanoparticles confined within aqueous droplete

机译:限制在水滴内的亚细胞细胞器和纳米颗粒的大小

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摘要

Ibis article describes two complementary techniques, single-particle tracking and correlation spectroscopy, for accurately sizing nanoparticles confined within picoliter volume aqueous droplets. Single-particle tracking works well with bright particles that can be continuously illuminated and imaged, and we demonstrated this approach for sizing single fluorescent beads. Fluorescence correlation spectroscopy detects small intensity bursts from particles or molecules diffusing through the confocal probe volume, which works well with dim and rapidly diffusing particles or molecules; we demonstrated FCS for sizing synaptic vesicles confined in aqueous droplets. In combination with recent advances in droplet manipulations and analysis, we anticipate this capability to size single nanoparticles and molecules in free solution will complement existing tools for probing cellular systems, subcellular organelles, and nanoparticles.
机译:Ibis文章描述了两种互补技术,即单颗粒跟踪和相关光谱,用于精确确定装在皮升体积的水滴内的纳米颗粒的尺寸。单粒子跟踪对于可以连续照明和成像的明亮粒子效果很好,并且我们演示了此方法来确定单个荧光珠的大小。荧光相关光谱法可检测到通过共聚焦探针体积扩散的粒子或分子产生的小强度爆发,这对于暗淡且快速扩散的粒子或分子效果很好。我们证明了FCS可用于确定封闭在水滴中的突触小泡的大小。结合液滴操作和分析的最新进展,我们预计这种在自由溶液中确定单个纳米颗粒和分子大小的能力将补充用于探测细胞系统,亚细胞器和纳米颗粒的现有工具。

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