Visualization of spatially and temporally regulated N-WASP activity during cytoskeletal reorganization in living cells
Author(s) -
Michael E. Ward,
Jane Y. Wu,
Yi Rao
Publication year - 2004
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0306258101
Subject(s) - microbiology and biotechnology , biology , cytoskeleton , filopodia , wiskott–aldrich syndrome protein , cdc42 , förster resonance energy transfer , membrane ruffling , actin , actin cytoskeleton , cell , genetics , physics , quantum mechanics , fluorescence
Members of the WASP/WAVE family of proteins are key regulators of cytoskeletal reorganization across a diverse range of cellular processes. Despite a wealth of biochemical data about WASP/WAVE regulation in vitro, our understanding of the in vivo regulation of these proteins is hampered by the inability to monitor subcellular regulation of their activities in living cells. Here we establish a fluorescence resonance energy transfer-based approach to visualize spatial and temporal regulation of neuronal Wiskott-Aldrich syndrome protein (N-WASP) activity in living cells. Using time-lapse microscopy, we characterize the activation of N-WASP in response to growth-factor stimulation, and we reveal that N-WASP is activated inside extending filopodia. Furthermore, we suggest a role of N-WASP in regulating membrane ruffling downstream of phosphatidylinositol 4,5-bisphosphate and Cdc42.
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