Abstract
During cell locomotion and endocytosis, membrane-tethered WASP proteins stimulate actin filament nucleation by the Arp2/3 complex. This process generates highly branched arrays of filaments that grow toward the membrane to which they are tethered, a conflict that seemingly would restrict filament growth. Using three-color single-molecule imaging in vitro we revealed how the dynamic associations of Arp2/3 complex with mother filament and WASP are temporally coordinated with initiation of daughter filament growth. We found that WASP proteins dissociated from filamentbound Arp2/3 complex prior to new filament growth. Further, mutations that accelerated release of WASP from filament-bound Arp2/3 complex proportionally accelerated branch formation. These data suggest that while WASP promotes formation of pre-nucleation complexes, filament growth cannot occur until it is triggered by WASP release. This provides a mechanism by which membrane-bound WASP proteins can stimulate network growth without restraining it. © Smith et al.
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CITATION STYLE
Smith, B. A., Padrick, S. B., Doolittle, L. K., Daugherty-Clarke, K., Corrêa, I. R., Xu, M. Q., … Gelles, J. (2013). Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation. ELife, 2013(2). https://doi.org/10.7554/eLife.01008
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