Parsons S J, McCarley D J, Ely C M, Benjamin D C, Parsons J T
J Virol. 1984 Aug;51(2):272-82. doi: 10.1128/JVI.51.2.272-282.1984.
The derivation and characterization of 22 hybridoma clones producing monoclonal antibodies (Mabs) specific for the transforming protein of Rous sarcoma virus, pp60src, are described. All Mabs reacted with pp60v-src encoded by Prague, Schmidt-Ruppin, and Bratislava 77 strains of Rous sarcoma virus. Of these Mabs, 10 efficiently immunoprecipitated pp60c-src from chicken embryo cells. Of these 10 Mabs, 2 (GD11 and EB8) readily detected pp60c-src from a variety of rodent and human cultured cells and from rat brain tissue in an in vitro immune complex kinase assay. Mapping experiments have tentatively localized the determinant(s) recognized by GD11 and EB8 to a region of the src protein bounded by amino acid residues 82 to 169, whereas the remaining Mabs appeared to recognize determinants residing within residues 1 to 82 or 169 to 173. Most of the Mabs complexed denatured pp60v-src in a Western immunoblot, and several were used to localize pp60v-src in Rous sarcoma virus-transformed chicken embryo cells by indirect immunofluorescence microscopy.
本文描述了22个杂交瘤克隆的衍生和特性,这些克隆产生针对劳氏肉瘤病毒转化蛋白pp60src的单克隆抗体(Mabs)。所有单克隆抗体都与由布拉格、施密特-鲁平及布拉迪斯拉发77株劳氏肉瘤病毒编码的pp60v-src发生反应。在这些单克隆抗体中,有10个能有效地从鸡胚细胞中免疫沉淀pp60c-src。在这10个单克隆抗体中,有2个(GD11和EB8)在体外免疫复合物激酶分析中能轻易地从多种啮齿动物和人类培养细胞以及大鼠脑组织中检测到pp60c-src。定位实验初步将GD11和EB8识别的决定簇定位到src蛋白中由氨基酸残基82至169界定的区域,而其余单克隆抗体似乎识别位于残基1至82或169至173内的决定簇。大多数单克隆抗体在蛋白质免疫印迹中与变性的pp60v-src形成复合物,并且有几种被用于通过间接免疫荧光显微镜在劳氏肉瘤病毒转化的鸡胚细胞中定位pp60v-src。