Until recently, cytoskeleton research has relied primarily on immunofl
uorescence microscopy techniques, requiring fixation and hence killing
of the specimen before the analysis. The sole method for visualizing
cytoskeletal dynamics in living cells has been tile microinjection of
purified and fluorescently labelled protein, brit technical difficulti
es have precluded its widespread use. The recent introduction of green
fluorescent protein (GFP) has enabled visualization of proteins and c
ytoskeletal dynamics with only minimal perturbations of the living cel
l and has opened new horizons for studying the cytoskeleton.