Gambke C, Senn H P, Hunsmann G, Schumann G, Moroni C, Alkan S S
J Gen Virol. 1984 Sep;65 ( Pt 9):1507-17. doi: 10.1099/0022-1317-65-9-1507.
Monoclonal antibodies were prepared from mice and rats immunized with Friend leukaemia virus and BALB/c xenotropic virus. By immunoprecipitation of 125I-labelled and [35S]methionine-labelled viruses and by protein blotting, ten antibodies were found to react with the viral components p12, p15, p30, gp70 and p15E/p12E. A dot-immunobinding assay was found to be a reliable method to type the antibody reactivity with different murine leukaemia viruses (MuLVs). When tested on a panel of ecotropic and xenotropic MuLVs the antibodies revealed the following antigenic specificities: ecotrop-specific on p15E/p12E; xenotrop-specific on p15E; group-specific on p30 and p15E; FM-specific on gp70; FR-specific on gp70 and p15. Of particular interest is a cytotoxic antibody recognizing an FMR determinant localized on p12.
用弗氏白血病病毒和BALB/c嗜异性病毒免疫小鼠和大鼠后制备单克隆抗体。通过对125I标记和[35S]甲硫氨酸标记病毒进行免疫沉淀以及蛋白质印迹法,发现有十种抗体与病毒成分p12、p15、p30、gp70和p15E/p12E发生反应。斑点免疫结合试验被认为是一种确定抗体与不同鼠白血病病毒(MuLVs)反应类型的可靠方法。当在一组嗜亲性和嗜异性MuLVs上进行测试时,这些抗体显示出以下抗原特异性:对p15E/p12E具有嗜亲性特异性;对p15E具有嗜异性特异性;对p30和p15E具有组特异性;对gp70具有FM特异性;对gp70和p15具有FR特异性。特别有趣的是一种细胞毒性抗体,它识别位于p12上的FMR决定簇。