One way to visualize and track the movement of macromolecules in the living
cell is to follow their movement after tagging the molecule with a 'caged'
or chemically masked fluorochrome. The fluorochrome does not fluoresce unt
il the caging group is released by spot photoactivation, and the bright flu
orescent signal can then be tracked as it moves into the dark surrounding a
rea of the cell. When coupled with rapid imaging microscopy, it is possible
to measure rates of movement as fast as macromolecular diffusion. This art
icle describes the use of photoactivatable fluorochromes to track the intra
cellular movement of boat proteins and nucleic acids and to track cell line
ages.