Imaging protein-protein interactions in living cells

被引:0
作者
Mark A. Hink
Ton Bisseling
Antonie J.W.G. Visser
机构
[1] Wageningen University,MicroSpectroscopy Centre
[2] Vrije Universiteit,Department of Structural Biology, Faculty of Earth and Life Sciences
来源
Plant Molecular Biology | 2002年 / 50卷
关键词
cells; FCS; fluorescence spectroscopy; FRET; protein-protein interactions;
D O I
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中图分类号
学科分类号
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.
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页码:871 / 883
页数:12
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