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

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 gr...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762362/
https://www.ncbi.nlm.nih.gov/pubmed/24015360
http://dx.doi.org/10.7554/eLife.01008
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author 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
author_facet 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
author_sort Smith, Benjamin A
collection PubMed
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 filament-bound 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. DOI: http://dx.doi.org/10.7554/eLife.01008.001
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spelling pubmed-37623622013-09-06 Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation 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 Biochemistry 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 filament-bound 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. DOI: http://dx.doi.org/10.7554/eLife.01008.001 eLife Sciences Publications, Ltd 2013-09-03 /pmc/articles/PMC3762362/ /pubmed/24015360 http://dx.doi.org/10.7554/eLife.01008 Text en Copyright © 2013, Smith et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry
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
Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation
title Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation
title_full Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation
title_fullStr Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation
title_full_unstemmed Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation
title_short Three-color single molecule imaging shows WASP detachment from Arp2/3 complex triggers actin filament branch formation
title_sort three-color single molecule imaging shows wasp detachment from arp2/3 complex triggers actin filament branch formation
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762362/
https://www.ncbi.nlm.nih.gov/pubmed/24015360
http://dx.doi.org/10.7554/eLife.01008
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