Monoclonal antibodies to the peplomer glycoprotein of coronavirus mouse hepatitis virus identify two subunits and detect a conformational change in the subunit released under mild alkaline conditions.
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Localization of mouse hepatitis virus nonstructural proteins and RNA synthesis indicates a role for late endosomes in viral replicationRole of Endocytosis and Low pH in Murine Hepatitis Virus Strain A59 Cell EntryCloning of the mouse hepatitis virus (MHV) receptor: expression in human and hamster cell lines confers susceptibility to MHVThe avian coronavirus infectious bronchitis virus undergoes direct low-pH-dependent fusion activation during entry into host cellsThe S2 subunit of the murine coronavirus spike protein is not involved in receptor binding.Amino acid substitutions in the S2 subunit of mouse hepatitis virus variant V51 encode determinants of host range expansionEnhanced virulence mediated by the murine coronavirus, mouse hepatitis virus strain JHM, is associated with a glycine at residue 310 of the spike glycoprotein.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.Analysis of murine coronavirus surface glycoprotein functions by using monoclonal antibodies.Conformational change of the coronavirus peplomer glycoprotein at pH 8.0 and 37 degrees C correlates with virus aggregation and virus-induced cell fusion.The N-terminal domain of the murine coronavirus spike glycoprotein determines the CEACAM1 receptor specificity of the virus strain.Cooperative involvement of the S1 and S2 subunits of the murine coronavirus spike protein in receptor binding and extended host range.Mapping of the coronavirus membrane protein domains involved in interaction with the spike protein.Assembly of spikes into coronavirus particles is mediated by the carboxy-terminal domain of the spike protein.Conformational changes in the spike glycoprotein of murine coronavirus are induced at 37 degrees C either by soluble murine CEACAM1 receptors or by pH 8.The ubiquitin-proteasome system plays an important role during various stages of the coronavirus infection cycle.Disulfide bonds in folding and transport of mouse hepatitis coronavirus glycoproteins.
P2860
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P2860
Monoclonal antibodies to the peplomer glycoprotein of coronavirus mouse hepatitis virus identify two subunits and detect a conformational change in the subunit released under mild alkaline conditions.
description
1990 nî lūn-bûn
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1990年の論文
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1990年論文
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1990年論文
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name
Monoclonal antibodies to the p ...... nder mild alkaline conditions.
@ast
Monoclonal antibodies to the p ...... nder mild alkaline conditions.
@en
type
label
Monoclonal antibodies to the p ...... nder mild alkaline conditions.
@ast
Monoclonal antibodies to the p ...... nder mild alkaline conditions.
@en
prefLabel
Monoclonal antibodies to the p ...... nder mild alkaline conditions.
@ast
Monoclonal antibodies to the p ...... nder mild alkaline conditions.
@en
P2093
P2860
P1433
P1476
Monoclonal antibodies to the p ...... nder mild alkaline conditions.
@en
P2093
J O Fleming
K V Holmes
L S Sturman
M J Buchmeier
P2860
P304
P407
P577
1990-06-01T00:00:00Z