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用抗水痘 - 带状疱疹病毒(VZV)抗原的单克隆抗体研究水痘 - 带状疱疹病毒(VZV)糖蛋白的合成与加工。

Synthesis and processing of glycoproteins of Varicella-Zoster virus (VZV) as studied with monoclonal antibodies to VZV antigens.

作者信息

Okuno T, Yamanishi K, Shiraki K, Takahashi M

出版信息

Virology. 1983 Sep;129(2):357-68. doi: 10.1016/0042-6822(83)90175-7.

Abstract

Varicella-Zoster virus (VZV) contains four major glycoproteins designated as gp 1(115K), gp 2(100-80K), gp 3(64K), and gp 5(55K) (K. Shiraki, T. Okuno, K. Yamanishi, and M. Takahashi, J. Gen. Virol. 61, 255-269, 1982). The present studies focused on the synthesis and processing of these glycoproteins using monoclonal antibodies. Twenty-seven hybridomas secreting monoclonal antibodies against VZV proteins have been established. The antibodies were characterized further by radioimmunoprecipitation with [35S]-methionine, [3H]glucosamine, [125I]labeled viral antigens followed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Twelve clones of these hybridomas produced antibodies to glycosylated polypeptides of VZV, which could be classified into three groups on the basis of the electrophoretic patterns. The first group reacted specifically with polypeptides with apparent molecular weights of 94K and 83K (both presumed to correspond to gp 2) in infected cells, on the surface membrane of infected cells, and on the virions. The second group precipiated polypeptides with molecular weights of 94K, 83K, 55K (corresponding to gp 5) in infected cells, and 94K, 83K, 55K, 45K on the surface membrane of infected cells, and 94K, 83K, and 55K on the virions. Finally, the third group reacted with polypeptides with molecular weights of 116K, 106K, and 64K corresponding to gp 3) in infected cells, 64K on the surface membrane of infected cells, and on the virions. By pulse-chase experiments, antibodies from the former two groups precipitated new polypeptides with molecular weights of 75K and 49K, respectively, which were presumed to be precursor proteins. These data suggest that the precursor proteins of gp 2, gp 3, and gp 5 are synthesized in infected cells, glycosylated, and the product proteins are expressed on the surface membrane of infected cells as well as on the virions. It was also found that a glycoprotein of 45K detected in culture fluid of infected cells (K. Shiraki and M. Takahashi, J. Gen. Virol. 61, 271-275, 1982) was derived from the polypeptide with molecular weight of 55K (gp 5).

摘要

水痘 - 带状疱疹病毒(VZV)含有四种主要糖蛋白,分别命名为gp 1(115K)、gp 2(100 - 80K)、gp 3(64K)和gp 5(55K)(K. 白木、T. 奥野、K. 山中、M. 高桥,《普通病毒学杂志》61卷,255 - 269页,1982年)。本研究利用单克隆抗体聚焦于这些糖蛋白的合成与加工。已建立了27个分泌抗VZV蛋白单克隆抗体的杂交瘤细胞系。通过用[35S] - 甲硫氨酸、[3H] - 葡糖胺、[125I]标记的病毒抗原进行放射免疫沉淀,随后进行十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE),对这些抗体进行了进一步表征。这些杂交瘤细胞系中的12个克隆产生了针对VZV糖基化多肽的抗体,根据电泳图谱可将其分为三组。第一组与感染细胞、感染细胞表面膜及病毒粒子中表观分子量为94K和83K(两者均推测对应于gp 2)的多肽特异性反应。第二组在感染细胞中沉淀分子量为94K、83K、55K(对应于gp 5)的多肽,在感染细胞表面膜上沉淀分子量为94K、83K、55K、45K的多肽,在病毒粒子中沉淀分子量为94K、83K和55K的多肽。最后,第三组与感染细胞中分子量为116K、106K和64K(对应于gp 3)的多肽反应,在感染细胞表面膜及病毒粒子中与64K的多肽反应。通过脉冲追踪实验,前两组的抗体分别沉淀了分子量为75K和49K的新多肽,推测它们为前体蛋白。这些数据表明,gp 2、gp 3和gp 5的前体蛋白在感染细胞中合成、糖基化,产物蛋白在感染细胞表面膜及病毒粒子上表达。还发现,在感染细胞培养液中检测到的45K糖蛋白(K. 白木和M. 高桥,《普通病毒学杂志》61卷,271 - 275页,1982年)源自分子量为55K的多肽(gp 5)。

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