Schneider J, Hunsmann G
Int J Cancer. 1978 Aug 15;22(2):204-13. doi: 10.1002/ijc.2910220215.
The expression of murine leukemia virus structural polypeptides on the surface of cells producing exogenous Friend leukemia virus, endogenous ecotropic AKR and xenotropic BALB/c virus was investigated. Antisera to Friend virus gp71, p30, p15E, p12 and p10 were employed in a complement-dependent chromium release assay and to immunoprecipitate lactoperoxidase iodinated surface polypeptides prior to analysis in polyacrylamide gel electrophoresis. With the latter technique gag-gene encoded proteins and their precursors were not discovered on the viral and cellular surface membranes. Only env-gene encoded polypeptides gp85, gp71, and p15E were detectable. p15E is embedded into the lipid membrane. gp85 is formed by disulfide linkage of p15E to surface-exposed gp71. The ratio of gp71 to gp85 is variable and apparently determined by the host cell. Antibodies of strong cytotoxicity are those against type- and group-specific epitopes of gp71 as well as type-specific epitopes of p12.
研究了鼠白血病病毒结构多肽在产生外源性Friend白血病病毒、内源性嗜亲性AKR病毒和异嗜性BALB/c病毒的细胞表面的表达情况。在补体依赖的铬释放试验中使用了针对Friend病毒gp71、p30、p15E、p12和p10的抗血清,并在聚丙烯酰胺凝胶电泳分析之前免疫沉淀乳过氧化物酶碘化的表面多肽。使用后一种技术,在病毒和细胞表面膜上未发现gag基因编码的蛋白质及其前体。仅可检测到env基因编码的多肽gp85、gp71和p15E。p15E嵌入脂质膜中。gp85由p15E与表面暴露的gp71通过二硫键连接形成。gp71与gp85的比例是可变的,显然由宿主细胞决定。具有强细胞毒性的抗体是针对gp71的型特异性和组特异性表位以及p12的型特异性表位的抗体。