Neutralization epitope of varicella zoster virus on native viral glycoprotein gp118 (VZV glycoprotein gpIII).
Neutralization epitope of varicella zoster virus on native viral glycoprotein gp118 (VZV glycoprotein gpIII).
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水痘带状疱疹病毒对天然病毒糖蛋白 gp118(VZV 糖蛋白 gpIII)的中和表位。
DOI:
10.1016/0042-6822(86)90124-8
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发表时间:
1986
期刊:
影响因子:
3.7
通讯作者:
Grose,C
中科院分区:
文献类型:
--
作者:
Montalvo,EA;Grose,C
Varicella-zoster virus (VZV) specifies the formation of several glycoproteins, including a 118,000-Da mature structural product (gp118). The biologic and biochemical properties of gp118 were studied after production of murine monoclonal antibodies to both a low-passage laboratory strain (VZV-32) and an attenuated vaccine strain (VZV-Oka). Structural analyses performed with the three glycosidases endo-(β-N-acetylglucosaminidase H (endoglycosidase H), endo-β-N-acetylglucosaminidase F (endoglycosidase F), and endo-α-N-acetylgalactosaminidase demonstrated that gp118 was predominantly an N-linked complex type glycoprotein built upon a polypeptide backbone of approximately 79,000 Da. Sialic acid residues were present on the mature glycoprotein, but these terminal sugars were absent from the partially glycosylated intermediate forms recovered from monensin-treated infected cultures. Unlike another VZV-specified glycoprotein gp98, no new oligosaccharide moieties were observed on gp118 after addition of tunicamycin to VZV-infected cultures. By plaque reduction assays with a panel of monoclonal antibodies, we defined an epitope on this glycoprotein which elicited a complement-independent neutralizing antibody response of high magnitude. The epitope was highly conserved, since it was present on a laboratory VZV strain, wild type isolates, as well as the attenuated vaccine strain (VZV-Oka). Competitive blocking experiments with the same anti-gp118 monoclonal antibodies indicated that four neutralizing antibodies were directed against similar or identical epitopes whereas one nonneutralizing antibody reacted with a different antigenic site. Thus, this study demonstrates the presence of an immunodominant neutralization epitope on native viral glycoprotein gp118. Under a new consensus nomenclature, this glycoprotein will be designated VZV gpIII.
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影响因子:
3.7
作者:
GROSE, C
通讯作者:
GROSE, C
影响因子:
5.4
作者:
R. Ellis;P. Keller;R. Lowe;R. Zivin
通讯作者:
R. Zivin
DOI:
10.1073/pnas.79.15.4540
发表时间:
1982-01-01
期刊:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES
影响因子:
--
作者:
ELDER, JH;ALEXANDER, S
通讯作者:
ALEXANDER, S
影响因子:
64.5
作者:
ROBBINS, PW;HUBBARD, SC;WIRTH, DF
通讯作者:
WIRTH, DF
影响因子:
5.4
作者:
BALACHANDRAN, N;HUTTFLETCHER, LM
通讯作者:
HUTTFLETCHER, LM