Real-Time Measurements of Protein Dynamics Using Fluorescence Activation-Coupled Protein Labeling Method

被引:110
作者
Komatsu, Toru [1 ,5 ]
Johnsson, Kai [3 ]
Okuno, Hiroyuki [2 ,5 ]
Bito, Haruhiko [2 ,5 ]
Inoue, Takanari [4 ]
Nagano, Tetsuo [1 ,5 ]
Urano, Yasuteru [1 ,2 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Med, Bunkyo Ku, Tokyo 1130033, Japan
[3] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
[4] Johns Hopkins Univ, Sch Med, Dept Cell Biol, Ctr Cell Dynam, Baltimore, MD 21205 USA
[5] JST CREST, Chiyoda Ku, Tokyo 1020075, Japan
关键词
FUSION PROTEINS; SMALL MOLECULES; BETA-LACTAMASE; LIVING CELLS; ENDOCYTOSIS; MULTICOLOR; RECEPTORS;
D O I
10.1021/ja200225m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present a fluorescence activation-coupled protein labeling (FAPL) method, which employs small-molecular probes that exhibit almost no basal fluorescence but acquire strong fluorescence upon covalent binding to tag-proteins. This method enables real-time imaging of protein labeling without any washout process and is uniquely suitable for real-time imaging of protein dynamics on the cell surface. We applied this method to address the spatiotemporal dynamics of the EGF receptor during cell migration.
引用
收藏
页码:6745 / 6751
页数:7
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