Fluorescent indicators for imaging protein phosphorylation in single living cells

被引:224
作者
Sato, M
Ozawa, T
Inukai, K
Asano, T
Umezawa, Y [1 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Corp, Tokyo 1130033, Japan
[3] Univ Tokyo, Sch Med, Dept Internal Med 3, Bunkyo Ku, Tokyo 1130033, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1038/nbt0302-287
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To visualize signal transduction based on protein phosphorylation in living cells, we have developed genetically encoded fluorescent indicators, named phocuses. Two different color mutants of green fluorescent protein (GFP) were joined by a tandem fusion domain composed of a substrate domain for the protein kinase of interest, a flexible linker sequence, and a phosphorylation recognition domain that binds with the phosphorylated substrate domain. Intramolecular interaction of the substrate domain and the adjacent phosphorylation recognition domain within a phocus was dependent upon phosphorylation of the substrate domain by protein kinase, which influenced the efficiency of fluorescence resonance energy transfer (FRET) between the GFPs within a phocus. In the present study, we employed phocuses composed of insulin signaling proteins to visualize protein phosphorylation by the insulin receptor. This method may provide a general approach for studying the dynamics of protein phosphorylation-based signal transduction in living cells.
引用
收藏
页码:287 / 294
页数:8
相关论文
共 47 条
  • [1] FLUORESCENCE RATIO IMAGING OF CYCLIC-AMP IN SINGLE CELLS
    ADAMS, SR
    HAROOTUNIAN, AT
    BUECHLER, YJ
    TAYLOR, SS
    TSIEN, RY
    [J]. NATURE, 1991, 349 (6311) : 694 - 697
  • [2] SINGLE-CHAIN ANTIGEN-BINDING PROTEINS
    BIRD, RE
    HARDMAN, KD
    JACOBSON, JW
    JOHNSON, S
    KAUFMAN, BM
    LEE, SM
    LEE, T
    POPE, SH
    RIORDAN, GS
    WHITLOW, M
    [J]. SCIENCE, 1988, 242 (4877) : 423 - 426
  • [3] Green fluorescent antibodies:: novel in vitro tools
    Casey, JL
    Coley, AM
    Tilley, LM
    Foley, M
    [J]. PROTEIN ENGINEERING, 2000, 13 (06): : 445 - 452
  • [4] Structure of the IRS-1 PTB domain bound to the juxtamembrane region of the insulin receptor
    Eck, MJ
    DhePaganon, S
    Trub, T
    Nolte, RT
    Shoelson, SE
    [J]. CELL, 1996, 85 (05) : 695 - 705
  • [5] GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
  • [6] Imaging of Ca2(+)/calmodulin-dependent protein kinase II activity in hippocampal neurones
    Higashi, H
    Sato, K
    Omori, A
    Sekiguchi, M
    Ohtake, A
    Kudo, Y
    [J]. NEUROREPORT, 1996, 7 (15-17) : 2695 - 2700
  • [7] Imaging of cAMP-dependent protein kinase activity in living neural cells using a novel fluorescent substrate
    Higashi, H
    Sato, K
    Ohtake, A
    Omori, A
    Yoshida, S
    Kudo, Y
    [J]. FEBS LETTERS, 1997, 414 (01): : 55 - 60
  • [8] Spatiotemporal dynamics of inositol 1,4,5-trisphosphate that underlies complex Ca2+ mobilization patterns
    Hirose, K
    Kadowaki, S
    Tanabe, M
    Takeshima, H
    Iino, M
    [J]. SCIENCE, 1999, 284 (5419) : 1527 - 1530
  • [9] Spatiotemporal dynamics of guanosine 3′,5′-cyclic monophosphate revealed by a genetically encoded, fluorescent indicator
    Honda, A
    Adams, SR
    Sawyer, CL
    Lev-Ram, V
    Tsien, RY
    Dostmann, WRG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) : 2437 - 2442
  • [10] Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analog
    Hubbard, SR
    [J]. EMBO JOURNAL, 1997, 16 (18) : 5572 - 5581