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Single-particle Tracking as a Quantitative Microscopy-based Approach to Unravel Cell Entry Mechanisms of Viruses and Pharmaceutical Nanoparticles

机译:单颗粒跟踪作为一种基于定量显微镜的方法来阐明病毒和药物纳米颗粒的细胞进入机制

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摘要

Highly sensitive fluorescence microscopy techniques allow single nanoparticles to be tracked during their uptake into living cells with high temporal and spatial resolution. From analysis of the trajectories, random motion can be discriminated from active transport and the average transport velocity and/or diffusion coefficient determined. Such an analysis provides important information regarding the uptake pathway and location of viruses and nanoparticles. In this review, we give an introduction into single-particle tracking (SPT) and determination of the mean-squared displacement. We also give an overview of recent advances in SPT. These include millisecond alternating-laser excitation for removal of spectral crosstalk, alternating wide-field (WF), and total internal reflection fluorescence (TIRF) microscopy for sensitive experiments at the plasma membrane and three-dimensional tracking strategies. Throughout the review, we highlight recent advances regarding the entry (and egress) of natural and artificial viruses obtained via SPT.
机译:高度灵敏的荧光显微镜技术使单个纳米颗粒在以高时间和空间分辨率进入活细胞的过程中得以追踪。通过轨迹分析,可以将随机运动与主动传输区分开,并确定平均传输速度和/或扩散系数。这样的分析提供了有关病毒和纳米颗粒的摄取途径和位置的重要信息。在这篇综述中,我们对单粒子跟踪(SPT)和均方位移的确定进行了介绍。我们还概述了SPT的最新进展。这些措施包括用于消除光谱串扰的毫秒级交替激光激发,交替的宽视场(WF)和全内反射荧光(TIRF)显微镜,用于质膜敏感的实验和三维跟踪策略。在整个审查过程中,我们重点介绍了通过SPT获得的天然和人工病毒进入(和流出)的最新进展。

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