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

被引:169
|
作者
Ruthardt, Nadia [1 ,2 ,3 ]
Lamb, Don C. [1 ,2 ,3 ,4 ]
Braeuchle, Christoph [1 ,2 ,3 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Chem, D-81377 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Ctr NanoSci CeNS, D-81377 Munich, Germany
[3] Ludwig Maximilians Univ Munchen, CIPSM, D-81377 Munich, Germany
[4] Univ Illinois, Dept Phys, Urbana, IL USA
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; ALTERNATING-LASER EXCITATION; IMAGE CORRELATION SPECTROSCOPY; INDIVIDUAL INFLUENZA-VIRUSES; NONVIRAL GENE DELIVERY; POINT-SPREAD FUNCTION; MEDIATED ENDOCYTOSIS; SPECKLE MICROSCOPY; LIVE CELLS; REAL-TIME;
D O I
10.1038/mt.2011.102
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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.
引用
收藏
页码:1199 / 1211
页数:13
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