Imaging protein-protein interactions in living cells

被引:105
作者
Hink, MA
Bisseling, T
Visser, AJWG
机构
[1] Wageningen Univ, Microspect Ctr, NL-6703 HA Wageningen, Netherlands
[2] Vrije Univ Amsterdam, Fac Earth & Life Sci, Dept Biol Struct, NL-1081 HV Amsterdam, Netherlands
关键词
cells; FCS; fluorescence spectroscopy; FRET; protein-protein interactions;
D O I
10.1023/A:1021282619035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The complex organization of plant cells makes it likely that the molecular behaviour of proteins in the test tube and the cell is different. For this reason, it is essential though a challenge to study proteins in their natural environment. Several innovative microspectroscopic approaches provide such possibilities, combining the high spatial resolution of microscopy with spectroscopic techniques to obtain information about the dynamical behaviour of molecules. Methods to visualize interaction can be based on FRET ( fluorescence detected resonance energy transfer), for example in fluorescence lifetime imaging microscopy (FLIM). Another method is based on fluorescence correlation spectroscopy (FCS) by which the diffusion rate of single molecules can be determined, giving insight into whether a protein is part of a larger complex or not. Here, both FRET- and FCS-based approaches to study protein-protein interactions in vivo are reviewed.
引用
收藏
页码:871 / 883
页数:13
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