SILAC-based proteomic quantification of chemoattractant-induced cytoskeleton dynamics on a second to minute timescale

被引:14
作者
Sobczyk, Grzegorz J. [1 ]
Wang, Jun [1 ]
Weijer, Cornelis J. [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Div Cell & Dev Biol, Dundee DD1 5EH, Scotland
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
ACTIN POLYMERIZATION; EUKARYOTIC CHEMOTAXIS; CELL POLARITY; MYOSIN-II; G-PROTEIN; DICTYOSTELIUM; RAS; ACTIVATION; FAMILY; IDENTIFICATION;
D O I
10.1038/ncomms4319
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cytoskeletal dynamics during cell behaviours ranging from endocytosis and exocytosis to cell division and movement is controlled by a complex network of signalling pathways, the full details of which are as yet unresolved. Here we show that SILAC-based proteomic methods can be used to characterize the rapid chemoattractant-induced dynamic changes in the actinmyosin cytoskeleton and regulatory elements on a proteome-wide scale with a second to minute timescale resolution. This approach provides novel insights in the ensemble kinetics of key cytoskeletal constituents and association of known and novel identified binding proteins. We validate the proteomic data by detailed microscopy-based analysis of in vivo translocation dynamics for key signalling factors. This rapid large-scale proteomic approach may be applied to other situations where highly dynamic changes in complex cellular compartments are expected to play a key role.
引用
收藏
页数:14
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