Herpes simplex virus immunoglobulin G Fc receptor activity depends on a complex of two viral glycoproteins, gE and gI.
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Crystal structure of the HSV-1 Fc receptor bound to Fc reveals a mechanism for antibody bipolar bridging.Antivirals reduce the formation of key Alzheimer's disease molecules in cell cultures acutely infected with herpes simplex virus type 1Cell-to-cell spread of wild-type herpes simplex virus type 1, but not of syncytial strains, is mediated by the immunoglobulin-like receptors that mediate virion entry, nectin1 (PRR1/HveC/HIgR) and nectin2 (PRR2/HveB)Characterization of Antibody Bipolar Bridging Mediated by the Human Cytomegalovirus Fc Receptor gp68The herpes virus Fc receptor gE-gI mediates antibody bipolar bridging to clear viral antigens from the cell surfaceComplement and its role in protection and pathogenesis of flavivirus infectionsGenital Herpes: Insights into Sexually Transmitted Infectious DiseaseReplication of herpes simplex virus: egress of progeny virus at specialized cell membrane sites.Herpes simplex virus membrane proteins gE/gI and US9 act cooperatively to promote transport of capsids and glycoproteins from neuron cell bodies into initial axon segments.The murine gammaherpesvirus-68 gp150 acts as an immunogenic decoy to limit virion neutralizationHuman cytomegalovirus Fcγ binding proteins gp34 and gp68 antagonize Fcγ receptors I, II and IIIHerpes simplex virus gD and virions accumulate in endosomes by mannose 6-phosphate-dependent and -independent mechanisms.In vivo immune evasion mediated by the herpes simplex virus type 1 immunoglobulin G Fc receptor.Herpes simplex virus type 1 glycoprotein gC mediates immune evasion in vivoThe herpes simplex virus gE-gI complex facilitates cell-to-cell spread and binds to components of cell junctionsThe extracellular domain of herpes simplex virus gE is sufficient for accumulation at cell junctions but not for cell-to-cell spread.Exploitation of herpesviral transactivation allows quantitative reporter gene-based assessment of virus entry and neutralization.Complement Evasion Strategies of Viruses: An Overview.Herpes simplex virus type 1 glycoprotein E domains involved in virus spread and diseaseTranscriptional analysis of Marek's disease virus glycoprotein D, I, and E genes: gD expression is undetectable in cell cultureMicrotubule reorganization during herpes simplex virus type 1 infection facilitates the nuclear localization of VP22, a major virion tegument proteinCytoplasmic domain of herpes simplex virus gE causes accumulation in the trans-Golgi network, a site of virus envelopment and sorting of virions to cell junctions.A novel herpes simplex virus glycoprotein, gL, forms a complex with glycoprotein H (gH) and affects normal folding and surface expression of gH.Identification and characterization of a novel herpes simplex virus glycoprotein, gK, involved in cell fusionThe capsid protein encoded by U(L)17 of herpes simplex virus 1 interacts with tegument protein VP13/14.The extracellular domain of herpes simplex virus gE is indispensable for efficient cell-to-cell spread: evidence for gE/gI receptorsHSV-1-based vectors for gene therapy of neurological diseases and brain tumors: part I. HSV-1 structure, replication and pathogenesis.Induction of immunoglobulin G Fc receptors by recombinant vaccinia viruses expressing glycoproteins E and I of herpes simplex virus type 1Herpes simplex virus gE/gI extracellular domains promote axonal transport and spread from neurons to epithelial cells.DNA cleavage and packaging proteins encoded by genes U(L)28, U(L)15, and U(L)33 of herpes simplex virus type 1 form a complex in infected cells.Ultrastructural localization of the herpes simplex virus type 1 UL31, UL34, and US3 proteins suggests specific roles in primary envelopment and egress of nucleocapsids.Herpes simplex virus gE/gI must accumulate in the trans-Golgi network at early times and then redistribute to cell junctions to promote cell-cell spread.Herpes simplex virus type 1 and 2 glycoprotein C prevents complement-mediated neutralization induced by natural immunoglobulin M antibody.The herpes simplex virus 1 IgG fc receptor blocks antibody-mediated complement activation and antibody-dependent cellular cytotoxicity in vivo.Axonal transport and sorting of herpes simplex virus components in a mature mouse visual system.Characterization of a UL49-null mutant: VP22 of herpes simplex virus type 1 facilitates viral spread in cultured cells and the mouse corneaHerpes simplex virus glycoproteins gB and gD function in a redundant fashion to promote secondary envelopmentNF-kappaB is required for apoptosis prevention during herpes simplex virus type 1 infectionHerpes simplex virus glycoproteins gD and gE/gI serve essential but redundant functions during acquisition of the virion envelope in the cytoplasm.Interaction and interdependent packaging of tegument protein UL11 and glycoprotein e of herpes simplex virus.
P2860
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P2860
Herpes simplex virus immunoglobulin G Fc receptor activity depends on a complex of two viral glycoproteins, gE and gI.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
Herpes simplex virus immunoglo ...... iral glycoproteins, gE and gI.
@en
type
label
Herpes simplex virus immunoglo ...... iral glycoproteins, gE and gI.
@en
prefLabel
Herpes simplex virus immunoglo ...... iral glycoproteins, gE and gI.
@en
P2093
P2860
P1433
P1476
Herpes simplex virus immunoglo ...... viral glycoproteins, gE and gI
@en
P2093
P2860
P304
P407
P577
1988-04-01T00:00:00Z