Fluorescence-Based Detection of Proteins and Their Interactions in Live Cells

被引:13
作者
Stoneman, Michael R. [1 ]
Raicu, Valerica [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Phys, Milwaukee, WI 53211 USA
[2] Univ Wisconsin, Dept Biol Sci, Milwaukee, WI 53211 USA
基金
美国国家科学基金会;
关键词
QUATERNARY STRUCTURE; IN-VIVO; MICROSCOPY; RECEPTOR; COLOCALIZATION; STRENGTH; GUIDE; TIME;
D O I
10.1021/acs.jpcb.3c01419
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Recentadvances in fluorescence-based microscopy techniques, suchas single molecule fluorescence, Fo''rster resonance energy transfer(FRET), fluorescence intensity fluctuations analysis, and super-resolutionmicroscopy have expanded our ability to study proteins in greaterdetail within their native cellular environment and to investigatethe roles that protein interactions play in biological functions,such as inter- and intracellular signaling and cargo transport. Inthis Perspective, we provide an up-to-date overview of the currentstate of the art in fluorescence-based detection of proteins and theirinteractions in living cells with an emphasis on recent developmentsthat have facilitated the characterization of the spatial and temporalorganization of proteins into oligomeric complexes in the presenceand absence of natural and artificial ligands. Further advancementsin this field will only deepen our understanding of the underlyingmechanisms of biological processes and help develop new therapeutictargets.
引用
收藏
页码:4708 / 4721
页数:14
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