Affiliation:
1. Université Paris Cité, CNRS, Institut Jacques Monod Paris France
2. The Francis Crick Institute London UK
3. Department of Infectious Disease Imperial College London UK
Abstract
AbstractActivation of the Arp2/3 complex by VCA‐motif‐bearing actin nucleation‐promoting factors results in the formation of “daughter” actin filaments branching off the sides of pre‐existing “mother” filaments. Alternatively, when stimulated by SPIN90, Arp2/3 directly nucleates “linear” actin filaments. Uncovering the similarities and differences between these two mechanisms is fundamental to understanding how actin cytoskeleton dynamics are regulated. Here, analysis of individual filaments reveals that, unexpectedly, the VCA motifs of WASP, N‐WASP, and WASH destabilize existing branches, as well as SPIN90‐Arp2/3 at linear filament ends. Furthermore, branch stabilizer cortactin and destabilizer GMF each have a similar impact on SPIN90‐activated Arp2/3. However, unlike branch junctions, SPIN90‐Arp2/3 at the ends of linear filaments is not destabilized by piconewton forces and does not become less stable with time. It thus appears that linear and branched Arp2/3‐generated filaments respond similarly to the regulatory proteins we have tested, albeit with some differences, but significantly differ in their responses to aging and mechanical stress. These kinetic differences likely reflect the small conformational differences recently reported between Arp2/3 in branch junctions and linear filaments and suggest that their turnover in cells may be differently regulated.
Funder
Agence Nationale de la Recherche
Cancer Research UK
European Research Council
Horizon 2020 Framework Programme
Wellcome Trust
Publisher
Springer Science and Business Media LLC
Subject
General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience
Cited by
14 articles.
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