Single-molecule imaging and tracking of molecular dynamics in living cells

被引:36
作者
Li, Nan [1 ,2 ]
Zhao, Rong [1 ,2 ]
Sun, Yahong [1 ,2 ]
Ye, Zi [1 ,2 ]
He, Kangmin [3 ,4 ]
Fang, Xiaohong [1 ,2 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Harvard Med Sch, Dept Cell Biol, Boston, MA 02115 USA
[4] Boston Childrens Hosp, Cellular & Mol Med Program, Boston, MA 02115 USA
基金
中国国家自然科学基金;
关键词
single-molecule imaging; single-molecule tracking; live-cell imaging; fluorescence microscopy; quantitative analysis; CLATHRIN-MEDIATED ENDOCYTOSIS; LIGHT-SHEET MICROSCOPY; PHOTOACTIVATABLE FLUORESCENT PROTEINS; PLANE ILLUMINATION MICROSCOPY; FACTOR-BETA RECEPTORS; LIVE MAMMALIAN-CELLS; PARTICLE TRACKING; QUANTUM DOTS; PLASMA-MEMBRANE; COATED-PIT;
D O I
10.1093/nsr/nww055
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Unlike the ensemble-averaging measurements, the single-molecule imaging and tracking (SMIT) in living cells provides the real-time quantitative information about the locations, kinetics, dynamics and interactions of individual molecules in their native environments with high spatiotemporal resolution and minimal perturbation. The past decade has witnessed a transforming development in the methods of SMIT with living cells, including fluorescent probes, labeling strategies, fluorescence microscopy, and detection and tracking algorithms. In this review, we will discuss these aspects with a particular focus on their recent advancements. We will then describe representative single-molecule studies to illustrate how the single-molecule approaches can be applied to monitor biomolecular interaction/reaction dynamics, and extract the molecular mechanistic information for different cellular systems.
引用
收藏
页码:739 / 760
页数:22
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