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Nature Methods 5, 155–157. Combines photoactivated localization microscopy and single-particle tracking to map molecular mobility in living cells.

Sparse photoactivation allows successive positions of individual labelled molecules to be linked into trajectories; activation of fresh subsets yields many tracks in living cells. This extends photoactivated localization microscopy from accumulated positions to mobility. For free two-dimensional diffusion with independent per-coordinate fluorescence localization precision $\sigma$, instantaneous frames give mean squared displacement $4D\Delta t+4{\sigma }^2$. Motion blur, tracking errors, confinement and photobleaching must be accounted for before assigning mobility classes.^[ref]