A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
about
Adenovirus-Mediated Expression of the p14 Fusion-Associated Small Transmembrane Protein Promotes Cancer Cell Fusion and Apoptosis In Vitro but Does Not Provide Therapeutic Efficacy in a Xenograft Mouse Model of CancerExtracellular annexins and dynamin are important for sequential steps in myoblast fusion.A library of mammalian effector modules for synthetic morphologyEnhanced fusion pore expansion mediated by the trans-acting Endodomain of the reovirus FAST proteins.Features of a spatially constrained cystine loop in the p10 FAST protein ectodomain define a new class of viral fusion peptides.Reovirus FAST protein transmembrane domains function in a modular, primary sequence-independent manner to mediate cell-cell membrane fusion.Proteomics analysis of the DF-1 chicken fibroblasts infected with avian reovirus strain S1133.Posttranslational modification of vesicular stomatitis virus glycoprotein, but not JNK inhibition, is the antiviral mechanism of SP600125The p14 FAST protein of reptilian reovirus increases vesicular stomatitis virus neuropathogenesis.Transcriptional restriction of human immunodeficiency virus type 1 gene expression in undifferentiated primary monocytesMyogenic differentiation triggers PML nuclear body loss and DAXX relocalization to chromocentres.Use of lentiviral vectors to deliver and express bicistronic transgenes in developing chicken embryos.Membrane perturbation elicits an IRF3-dependent, interferon-independent antiviral response.Efficient reovirus- and measles virus-mediated pore expansion during syncytium formation is dependent on annexin A1 and intracellular calcium.Helix-destabilizing, beta-branched, and polar residues in the baboon reovirus p15 transmembrane domain influence the modularity of FAST proteins.Aquareovirus effects syncytiogenesis by using a novel member of the FAST protein family translated from a noncanonical translation start site.Reovirus FAST Protein Enhances Vesicular Stomatitis Virus Oncolytic Virotherapy in Primary and Metastatic Tumor Models.Multifaceted sequence-dependent and -independent roles for reovirus FAST protein cytoplasmic tails in fusion pore formation and syncytiogenesis.
P2860
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P2860
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
description
2008 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մարտին հրատարակված գիտական հոդված
@hy
article scientifique (publié 2008/03/07)
@fr
articolo scientifico (pubblicato il 2008/03/07)
@it
artigo científico (publicado na 2008/03/07)
@pt
artículu científicu espublizáu en 2008
@ast
im März 2008 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 7 March 2008)
@en
vedecký článok (publikovaný 2008/03/07)
@sk
videnskabelig artikel (udgivet 2008/03/07)
@da
name
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@ast
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@en
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@nl
type
label
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@ast
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@en
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@nl
prefLabel
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@ast
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@en
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@nl
P2093
P2860
P1433
P1476
A Virus-Encoded Cell–Cell Fusion Machine Dependent on Surrogate Adhesins
@en
P2093
Christopher Barry
Jayme Salsman
Roy Duncan
P2860
P304
P356
10.1371/JOURNAL.PPAT.1000016
P577
2008-03-07T00:00:00Z