Intracellular transport of recombinant coronavirus spike proteins: implications for virus assembly.
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The Severe Acute Respiratory Syndrome (SARS)-coronavirus 3a protein may function as a modulator of the trafficking properties of the spike proteinAssembly of the coronavirus envelope: homotypic interactions between the M proteinsMonoclonal antibody analysis of neutralization and antibody-dependent enhancement of feline infectious peritonitis virusMonoclonal antibodies to the spike protein of feline infectious peritonitis virus mediate antibody-dependent enhancement of infection of feline macrophagesAssembly of coronavirus spike protein into trimers and its role in epitope expressionIntracellular complexes of viral spike and cellular receptor accumulate during cytopathic murine coronavirus infections.Expression of the two major envelope proteins of equine arteritis virus as a heterodimer is necessary for induction of neutralizing antibodies in mice immunized with recombinant Venezuelan equine encephalitis virus replicon particles.Infectious bronchitis virus E protein is targeted to the Golgi complex and directs release of virus-like particles.Variations in disparate regions of the murine coronavirus spike protein impact the initiation of membrane fusion.Dissecting virus entry: replication-independent analysis of virus binding, internalization, and penetration using minimal complementation of β-galactosidaseIntracellular targeting signals contribute to localization of coronavirus spike proteins near the virus assembly site.A novel severe acute respiratory syndrome coronavirus protein, U274, is transported to the cell surface and undergoes endocytosis.The avian coronavirus infectious bronchitis virus undergoes direct low-pH-dependent fusion activation during entry into host cellsGenome sequence of torovirus identified from a pig with porcine epidemic diarrhea virus from the United States.Incorporation of spike and membrane glycoproteins into coronavirus virions.Nucleocapsid-independent assembly of coronavirus-like particles by co-expression of viral envelope protein genes.The S2 subunit of the murine coronavirus spike protein is not involved in receptor binding.The human immunodeficiency virus-1 nef gene product: a positive factor for viral infection and replication in primary lymphocytes and macrophages.Envelope glycoprotein interactions in coronavirus assemblyIdentification of spike protein residues of murine coronavirus responsible for receptor-binding activity by use of soluble receptor-resistant mutants.Localization of neutralizing epitopes and the receptor-binding site within the amino-terminal 330 amino acids of the murine coronavirus spike proteinMajor receptor-binding and neutralization determinants are located within the same domain of the transmissible gastroenteritis virus (coronavirus) spike proteinIdentification of an immunodominant linear neutralization domain on the S2 portion of the murine coronavirus spike glycoprotein and evidence that it forms part of complex tridimensional structure.Fusion formation by the uncleaved spike protein of murine coronavirus JHMV variant cl-2.Alteration of the pH dependence of coronavirus-induced cell fusion: effect of mutations in the spike glycoprotein.Analysis of murine coronavirus surface glycoprotein functions by using monoclonal antibodies.A review of genetic methods and models for analysis of coronavirus-induced severe pneumonitis.Differential role for low pH and cathepsin-mediated cleavage of the viral spike protein during entry of serotype II feline coronaviruses.Coronavirus genetically redirected to the epidermal growth factor receptor exhibits effective antitumor activity against a malignant glioblastomaCleavage of group 1 coronavirus spike proteins: how furin cleavage is traded off against heparan sulfate binding upon cell culture adaptation.A subset of porcine reproductive and respiratory syndrome virus GP3 glycoprotein is released into the culture medium of cells as a non-virion-associated and membrane-free (soluble) form.Assembly of spikes into coronavirus particles is mediated by the carboxy-terminal domain of the spike protein.Amino acid substitutions within the leucine zipper domain of the murine coronavirus spike protein cause defects in oligomerization and the ability to induce cell-to-cell fusion.Organization of two transmissible gastroenteritis coronavirus membrane protein topologies within the virion and core.Characterization of two new structural glycoproteins, GP(3) and GP(4), of equine arteritis virusTranslation but not the encoded sequence is essential for the efficient propagation of the defective interfering RNAs of the coronavirus mouse hepatitis virusA role for naturally occurring variation of the murine coronavirus spike protein in stabilizing association with the cellular receptor.The function of the spike protein of mouse hepatitis virus strain A59 can be studied on virus-like particles: cleavage is not required for infectivity.Fusion-defective mutants of mouse hepatitis virus A59 contain a mutation in the spike protein cleavage signal.Assembly of empty capsids by using baculovirus recombinants expressing human parvovirus B19 structural proteins.
P2860
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P2860
Intracellular transport of recombinant coronavirus spike proteins: implications for virus assembly.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年学术文章
@wuu
1990年学术文章
@zh-cn
1990年学术文章
@zh-hans
1990年学术文章
@zh-my
1990年学术文章
@zh-sg
1990年學術文章
@yue
1990年學術文章
@zh
1990年學術文章
@zh-hant
name
Intracellular transport of rec ...... plications for virus assembly.
@en
type
label
Intracellular transport of rec ...... plications for virus assembly.
@en
prefLabel
Intracellular transport of rec ...... plications for virus assembly.
@en
P2093
P2860
P1433
P1476
Intracellular transport of rec ...... plications for virus assembly.
@en
P2093
Horzinek MC
Zijderveld A
P2860
P304
P407
P577
1990-01-01T00:00:00Z