A bleached grid (top) can be compared with movement of individual NPCs (bottom).

In the first in vivo characterization of nuclear pore complex (NPC) dynamics in mammalian cells, Daigle et al. (page 71; see also the Comment on page 17) have found that NPCs are remarkably stable complexes that appear to be anchored to a protein network in the nuclear envelope. The work also demonstrates the feasibility of tracking single protein complexes in living cells.

By fusing GFP tags to POM121, lamin B1, or Nup153, the authors were able to track the movement and turnover of NPCs directly. Instead of diffusing freely within the plane of the nuclear envelope during interphase, NPCs remained largely immobile, only moving slowly in unison in large arrays. Individual subunits of the NPC vary considerably in their turnover rates, with POM121 turning over less than once per cell cycle,...

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