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Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation

eLife, ISSN: 2050-084X, Vol: 2013, Issue: 2, Page: e01008
2013
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Article Description

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.

Bibliographic Details

http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84884697646&origin=inward; http://dx.doi.org/10.7554/elife.01008; http://www.ncbi.nlm.nih.gov/pubmed/24015360; https://elifesciences.org/articles/01008#tbl1; http://dx.doi.org/10.7554/elife.01008.014; https://elifesciences.org/articles/01008#fig4; http://dx.doi.org/10.7554/elife.01008.011; https://elifesciences.org/articles/01008#decision-letter; http://dx.doi.org/10.7554/elife.01008.022; https://elifesciences.org/articles/01008#fig6; http://dx.doi.org/10.7554/elife.01008.019; https://elifesciences.org/articles/01008#fig2; http://dx.doi.org/10.7554/elife.01008.004; https://elifesciences.org/articles/01008#fig3; http://dx.doi.org/10.7554/elife.01008.010; https://elifesciences.org/articles/01008#fig5; http://dx.doi.org/10.7554/elife.01008.015; https://elifesciences.org/articles/01008#digest; http://dx.doi.org/10.7554/elife.01008.002; https://elifesciences.org/articles/01008#media1; http://dx.doi.org/10.7554/elife.01008.009; https://elifesciences.org/articles/01008#fig1; http://dx.doi.org/10.7554/elife.01008.003; https://elifesciences.org/articles/01008#abstract; http://dx.doi.org/10.7554/elife.01008.001; https://elifesciences.org/articles/01008; https://cdn.elifesciences.org/articles/01008/elife-01008-v1.pdf; https://cdn.elifesciences.org/articles/01008/elife-01008-v1.xml; https://elifesciences.org/articles/01008#fig7; http://dx.doi.org/10.7554/elife.01008.021; https://facultyopinions.com/prime/718112312#eval793483856; http://dx.doi.org/10.3410/f.718112312.793483856; http://dx.doi.org/10.7554/elife.01008.023; https://elifesciences.org/articles/01008#author-response; https://dx.doi.org/10.7554/elife.01008

Smith, Benjamin A; Padrick, Shae B; Doolittle, Lynda K; Daugherty-Clarke, Karen; Corrêa, Ivan R; Xu, Ming-Qun; Goode, Bruce L; Rosen, Michael K; Gelles, Jeff

eLife Sciences Organisation, Ltd.

Neuroscience; Biochemistry, Genetics and Molecular Biology; Immunology and Microbiology

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