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  • 1
    Publication Date: 2009-03-06
    Description: Understanding cell motility will require detailed knowledge not only of the localization of signalling networks regulating actin polymerization, but also of their dynamics. Unfortunately, many signalling networks are not amenable to such analysis, as they are frequently transient and dispersed. By contrast, the signalling pathways used by pathogens undergoing actin-based motility are highly localized and operate in a constitutive fashion. Taking advantage of this, we have analysed the dynamics of neuronal Wiskott-Aldrich syndrome protein (N-WASP), WASP-interacting protein (WIP), GRB2 and NCK, which are required to stimulate actin-related protein (ARP)2/3-complex-dependent actin-based motility of vaccinia virus, using fluorescence recovery after photobleaching. Here we show that all four proteins are rapidly exchanging, albeit at different rates, and that the turnover of N-WASP depends on its ability to stimulate ARP2/3-complex-mediated actin polymerization. Conversely, disruption of the interaction of N-WASP with GRB2 and/or the barbed ends of actin filaments increases its exchange rate and results in a faster rate of virus movement. We suggest that the exchange rate of N-WASP controls the rate of ARP2/3-complex-dependent actin-based motility by regulating the extent of actin polymerization by antagonizing filament capping.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weisswange, Ina -- Newsome, Timothy P -- Schleich, Sibylle -- Way, Michael -- Cancer Research UK/United Kingdom -- England -- Nature. 2009 Mar 5;458(7234):87-91. doi: 10.1038/nature07773.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Motility Laboratory, Cancer Research UK, London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19262673" target="_blank"〉PubMed〈/a〉
    Keywords: Actin-Related Protein 2-3 Complex/*metabolism ; Actins/chemistry/*metabolism ; Adaptor Proteins, Signal Transducing ; Biopolymers/chemistry/metabolism ; Cell Line ; Cytoskeletal Proteins/genetics/metabolism ; GRB2 Adaptor Protein/genetics/metabolism ; HeLa Cells ; Humans ; Intracellular Signaling Peptides and Proteins/genetics/metabolism ; Oncogene Proteins/genetics/metabolism ; Vaccinia virus/genetics ; Wiskott-Aldrich Syndrome Protein, Neuronal/genetics/*metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2004-08-07
    Description: The cascade of events that leads to vaccinia-induced actin polymerization requires Src-dependent tyrosine phosphorylation of the viral membrane protein A36R. We found that a localized outside-in signaling cascade induced by the viral membrane protein B5R is required to potently activate Src and induce A36R phosphorylation at the plasma membrane. In addition, Src-mediated phosphorylation of A36R regulated the ability of virus particles to recruit and release conventional kinesin. Thus, Src activity regulates the transition between cytoplasmic microtubule transport and actin-based motility at the plasma membrane.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Newsome, Timothy P -- Scaplehorn, Niki -- Way, Michael -- New York, N.Y. -- Science. 2004 Oct 1;306(5693):124-9. Epub 2004 Aug 5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Motility Laboratory, Room 529, Cancer Research UK, London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15297625" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/*metabolism ; Animals ; Cell Line ; Cell Membrane/metabolism/virology ; Chickens ; Consensus Sequence ; Enzyme Activation ; HeLa Cells ; Humans ; Kinesin/metabolism ; Membrane Glycoproteins/chemistry/metabolism ; Microtubules/*metabolism ; Phosphorylation ; Phosphotyrosine/metabolism ; Recombinant Fusion Proteins/metabolism ; Vaccinia virus/genetics/*metabolism/physiology ; Viral Envelope Proteins/chemistry/metabolism ; Viral Structural Proteins/*metabolism ; Virion/metabolism ; src-Family Kinases/*metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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