Visualization of molecular activities inside living cells with fluorescent labels

被引:45
作者
Bunt, G
Wouters, FS
机构
[1] Max Planck Inst Expt Med, D-37075 Gottingen, Germany
[2] European Neurosci Inst Gottingen, Cell Biophys Grp, Gottingen, Germany
来源
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL. 237 | 2004年 / 237卷
关键词
FRET; GFP; protein-protein interactions; biosensors; fluorescence; microscopy;
D O I
10.1016/S0074-7696(04)37005-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The major task of modern cell biology is to identify the function and relation of the many different gene products, discovered by genomics and proteomics approaches, in the context of the living cell. To achieve this goal, an increasing toolbox of custom-designed biosensors based on fluorescent labels is available to study the molecular activities of the cellular machinery. An overview of the current status of the young field of molecular-cellular physiology is presented that includes the application of fluorescent labels in the design of biosensors and the major detection schemes used to extract their sensing information. In particular, the use of the photophysical phenomenon of Forster resonance energy transfer (FRET) as a powerful indicator of cellular biochemical events is discussed. In addition, we will point out the challenges and directions of the field and project the short-term future for the application of fluorescence-based biosensors in biology.
引用
收藏
页码:205 / +
页数:80
相关论文
共 245 条
  • [1] Green fluorescent protein as a scaffold for intracellular presentation of peptides
    Abedi, MR
    Caponigro, G
    Kamb, A
    [J]. NUCLEIC ACIDS RESEARCH, 1998, 26 (02) : 623 - 630
  • [2] New biarsenical Ligands and tetracysteine motifs for protein labeling in vitro and in vivo: Synthesis and biological applications
    Adams, SR
    Campbell, RE
    Gross, LA
    Martin, BR
    Walkup, GK
    Yao, Y
    Llopis, J
    Tsien, RY
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (21) : 6063 - 6076
  • [3] 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
  • [4] Nanocrystal targeting in vivo
    Åkerman, ME
    Chan, WCW
    Laakkonen, P
    Bhatia, SN
    Ruoslahti, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) : 12617 - 12621
  • [5] Actin filament uncapping localizes to ruffling lamellae and rocketing vesicles
    Allen, PG
    [J]. NATURE CELL BIOLOGY, 2003, 5 (11) : 972 - 979
  • [6] Amini F, 2002, ANGEW CHEM INT EDIT, V41, P356, DOI 10.1002/1521-3773(20020118)41:2<356::AID-ANIE356>3.0.CO
  • [7] 2-M
  • [8] An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein
    Ando, R
    Hama, H
    Yamamoto-Hino, M
    Mizuno, H
    Miyawaki, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) : 12651 - 12656
  • [9] Spatio-temporal regulation of Rac1 and Cdc42 activity during nerve growth factor-induced neurite outgrowth in PC12 cells
    Aoki, K
    Nakamura, T
    Matsuda, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (01) : 713 - 719
  • [10] A genetically targetable fluorescent probe of channel gating with rapid kinetics
    Ataka, K
    Pieribone, VA
    [J]. BIOPHYSICAL JOURNAL, 2002, 82 (01) : 509 - 516