Imaging protein behavior inside the living cell

被引:15
作者
Day, RN [1 ]
机构
[1] Univ Virginia Hlth Syst, Dept Med, Charlottesville, VA 22908 USA
[2] Univ Virginia Hlth Syst, Dept Cell Biol, Charlottesville, VA 22908 USA
关键词
bioimaging; quantitative fluorescence microscopy; green fluorescent protein; nuclear structure; FRET; FLIM;
D O I
10.1016/j.mce.2004.10.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The genetically encoded fluorescent proteins (FPs) have transformed studies in cell biology by allowing the behavior of proteins to be tracked within the natural environment of the living cell. Progressively more complex imaging methods are being used to measure the mobility, co-localization and interactions of proteins labeled with the FPs. This review provides an overview of recent developments in live-cell imaging techniques to analyze the subcellular distribution and interactions of proteins in living cells. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 53 条
[1]   To 5D and beyond: Quantitative fluorescence microscopy in the postgenomic era [J].
Andrews, PD ;
Harper, IS ;
Swedlow, JR .
TRAFFIC, 2002, 3 (01) :29-36
[2]   Fluorescence lifetime imaging microscopy: spatial resolution of biochemical processes in the cell [J].
Bastiaens, PIH ;
Squire, A .
TRENDS IN CELL BIOLOGY, 1999, 9 (02) :48-52
[3]   Imaging the intracellular trafficking and state of the AB(5) quaternary structure of cholera toxin [J].
Bastiaens, PIH ;
Majoul, IV ;
Verveer, PJ ;
Soling, HD ;
Jovin, TM .
EMBO JOURNAL, 1996, 15 (16) :4246-4253
[4]   Microspectroscopic imaging tracks the intracellular processing of a signal transduction protein: Fluorescent-labeled protein kinase C beta I [J].
Bastiaens, PIH ;
Jovin, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8407-8412
[5]  
Berland Keith M, 2004, Methods Mol Biol, V261, P383
[6]   FRET or no FRET: A quantitative comparison [J].
Berney, C ;
Danuser, G .
BIOPHYSICAL JOURNAL, 2003, 84 (06) :3992-4010
[7]  
Centonze VE, 2003, METHOD ENZYMOL, V360, P542
[8]   Characterization of two-photon excitation fluorescence lifetime imaging microscopy for protein localization [J].
Chen, YE ;
Periasamy, A .
MICROSCOPY RESEARCH AND TECHNIQUE, 2004, 63 (01) :72-80
[9]   Graphical representation and multicomponent analysis of single-frequency fluorescence lifetime imaging microscopy data [J].
Clayton, AHA ;
Hanley, QS ;
Verveer, PJ .
JOURNAL OF MICROSCOPY-OXFORD, 2004, 213 (01) :1-5
[10]  
Clegg RM, 2003, METHOD ENZYMOL, V360, P509