Literature DB >> 10801131

Direct observation of dendritic actin filament networks nucleated by Arp2/3 complex and WASP/Scar proteins.

L Blanchoin1, K J Amann, H N Higgs, J B Marchand, D A Kaiser, T D Pollard.   

Abstract

Most nucleated cells crawl about by extending a pseudopod that is driven by the polymerization of actin filaments in the cytoplasm behind the leading edge of the plasma membrane. These actin filaments are linked into a network by Y-branches, with the pointed end of each filament attached to the side of another filament and the rapidly growing barbed end facing forward. Because Arp2/3 complex nucleates actin polymerization and links the pointed end to the side of another filament in vitro, a dendritic nucleation model has been proposed in which Arp2/3 complex initiates filaments from the sides of older filaments. Here we report, by using a light microscopy assay, many new features of the mechanism. Branching occurs during, rather than after, nucleation by Arp2/3 complex activated by the Wiskott-Aldrich syndrome protein (WASP) or Scar protein; capping protein and profilin act synergistically with Arp2/3 complex to favour branched nucleation; phosphate release from aged actin filaments favours dissociation of Arp2/3 complex from the pointed ends of filaments; and branches created by Arp2/3 complex are relatively rigid. These properties result in the automatic assembly of the branched actin network after activation by proteins of the WASP/Scar family and favour the selective disassembly of proximal regions of the network.

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Year:  2000        PMID: 10801131     DOI: 10.1038/35010008

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  205 in total

Review 1.  Actin-based motility of intracellular microbial pathogens.

Authors:  M B Goldberg
Journal:  Microbiol Mol Biol Rev       Date:  2001-12       Impact factor: 11.056

2.  Cryptosporidium parvum infection requires host cell actin polymerization.

Authors:  D A Elliott; D J Coleman; M A Lane; R C May; L M Machesky; D P Clark
Journal:  Infect Immun       Date:  2001-09       Impact factor: 3.441

3.  Direct real-time observation of actin filament branching mediated by Arp2/3 complex using total internal reflection fluorescence microscopy.

Authors:  K J Amann; T D Pollard
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-11       Impact factor: 11.205

4.  Arp2/3 complex requires hydrolyzable ATP for nucleation of new actin filaments.

Authors:  M J Dayel; E A Holleran; R D Mullins
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-18       Impact factor: 11.205

5.  Growth of branched actin networks against obstacles.

Authors:  A E Carlsson
Journal:  Biophys J       Date:  2001-10       Impact factor: 4.033

6.  Self-organization of a propulsive actin network as an evolutionary process.

Authors:  I V Maly; G G Borisy
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-25       Impact factor: 11.205

7.  ATP-dependent membrane assembly of F-actin facilitates membrane fusion.

Authors:  A Jahraus; M Egeberg; B Hinner; A Habermann; E Sackman; A Pralle; H Faulstich; V Rybin; H Defacque; G Griffiths
Journal:  Mol Biol Cell       Date:  2001-01       Impact factor: 4.138

8.  Profilin I is essential for cell survival and cell division in early mouse development.

Authors:  W Witke; J D Sutherland; A Sharpe; M Arai; D J Kwiatkowski
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

9.  Betacap73-ARF6 interactions modulate cell shape and motility after injury in vitro.

Authors:  Kathleen N Riley; Angel E Maldonado; Patrice Tellier; Crislyn D'Souza-Schorey; Ira M Herman
Journal:  Mol Biol Cell       Date:  2003-07-11       Impact factor: 4.138

10.  Convolution theory for dynamic systems: a bottom-up approach to the viscoelasticity of polymeric networks.

Authors:  Yann von Hansen; Sebastian Rode; Roland R Netz
Journal:  Eur Phys J E Soft Matter       Date:  2013-12-11       Impact factor: 1.890

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