Localized Rac activation dynamics visualized in living cells

被引:548
作者
Kraynov, VS
Chamberlain, C
Bokoch, GM
Schwartz, MA
Slabaugh, S
Hahn, KM [1 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Vasc Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1126/science.290.5490.333
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
Signaling proteins are thought to be tightly regulated spatially and temporally in order to generate specific and Localized effects. For Rac and other small guanosine triphosphatases, binding to guanosine triphosphate Leads to interaction with downstream targets and regulates subcellular localization. A method called FLAIR (fluorescence activation indicator for Rho proteins) was developed to quantify the spatio-temporal dynamics of the Rad nucleotide state in Living cells. FLAIR revealed precise spatial control of growth factor-induced Rac activation, in membrane ruffles and in a gradient of activation at the leading edge of motile cells. FLAIR exemplifies a generally applicable approach for examining spatio-temporal control of protein activity.
引用
收藏
页码:333 / 337
页数:5
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