The localization of Arp2/3 (white) in lamellipodia (top) is disrupted by tropomyosin (bottom).
Previously, the team examined the lamella and lamellipodia using quantitative fluorescent speckle microscopy (qFSM), a technique that allows for deconvolution of images of physically overlapping cell domains. The domains have distinct molecular components, filament–assembly kinetics, and motion. Moreover, although the lamellipodia moved forward and backward repeatedly in the axis of cell movement, the team saw hints that cells made forward progress only when...
The Rockefeller University Press
2005
The Rockefeller University Press
2005
You do not currently have access to this content.
