DYNAMIC IMAGING OF HOMO-FRET IN LIVE CELLS BY FLUORESCENCE ANISOTROPY MICROSCOPY

被引:37
作者
Ghosh, Subhasri [1 ]
Saha, Suvrajit [1 ]
Goswami, Debanjan [1 ]
Bilgrami, Sameera [2 ]
Mayor, Satyajit [1 ]
机构
[1] Natl Ctr Biol Sci, Bangalore, Karnataka, India
[2] Univ Calif San Diego, Dept Pathol, San Diego, CA 92103 USA
来源
METHODS IN ENZYMOLOGY, VOL 505: IMAGING AND SPECTROSCOPIC ANALYSIS OF LIVING CELLS: LIVE CELL IMAGING OF CELLULAR ELEMENTS AND FUNCTIONS | 2012年 / 505卷
基金
英国惠康基金;
关键词
GPI-ANCHORED PROTEINS; ENERGY-TRANSFER; LIVING CELLS; NANOSCALE ORGANIZATION; ORIENTATION FACTOR; HETEROGENEITY; MOLECULES; PROBE; GFP;
D O I
10.1016/B978-0-12-388448-0.00024-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multiple lipid and protein components of the plasma membrane of a living cell are organized, both compositionally and functionally, at different spatial and temporal scales. For instance, Rab protein domains in membranes the clathrin-coated pit, or the immunological synapse are exquisite examples of functional compartmentalization in cell membranes. These assemblies consist in part of nanoscale complexes of lipids and proteins and are necessary to facilitate some specific sorting and signaling functions. It is evident that cellular functions require a regulated spatiotemporal organization of components at the nanoscale, often comprising of countable number of molecular species. Here, we describe multiple homo-FRET-based imaging methods that provide information about nanoscale interactions between fluorescently tagged molecules in live cells, at optically resolved spatial resolution.
引用
收藏
页码:291 / 327
页数:37
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