Mapping Intracellular Diffusion Distribution Using Single Quantum Dot Tracking: Compartmentalized Diffusion Defined by Endoplasmic Reticulum

被引:56
|
作者
Li, Hui [1 ]
Dou, Shuo-Xing [1 ]
Liu, Yu-Ru [1 ]
Li, Wei [1 ]
Xie, Ping [1 ]
Wang, Wei-Chi [1 ]
Wang, Peng-Ye [1 ]
机构
[1] Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, Key Lab Soft Matter Phys, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; LIVING CELLS; MAMMALIAN-CELLS; LIVE CELLS; CYTOPLASM; MEMBRANE; VISCOSITY; DYNAMICS; CYTOARCHITECTURE; MACROMOLECULES;
D O I
10.1021/ja511273c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The crowded intracellular environment influences the diffusion-mediated cellular processes, such as metabolism, signaling, and transport. The hindered diffusion of macromolecules in heterogeneous cytoplasm has been studied over years, but the detailed diffusion distribution and its origin still remain unclear. Here, we introduce a novel method to map rapidly the diffusion distribution in single cells based on single-particle tracking (SPT) of quantum dots (QDs). The diffusion map reveals the heterogeneous intracellular environment and, more importantly, an unreported compartmentalization of QD diffusions in cytoplasm. Simultaneous observations of QD motion and green fluorescent protein-tagged endoplasmic reticulum (ER) dynamics provide direct evidence that the compartmentalization results from micron-scale domains defined by ER tubules, and ER cisternae form perinuclear areas that restrict QDs to enter. The same phenomenon was observed using fluorescein isothiocyanate-dextrans, further confirming the compartmentalized diffusion. These results shed new light on the diffusive movements of macromolecules in the cell, and the mapping of intracellular diffusion distribution may be used to develop strategies for nanoparticle-based drug deliveries and therapeutics.
引用
收藏
页码:436 / 444
页数:9
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