Surovac V M, Adomaĭtene D Iu
Ukr Biokhim Zh (1978). 1991 Jul-Aug;63(4):29-36.
After elimination of the virus fraction non-associated with bovine leukemia virus (free) glycoprotein gp-51 antigen has been preparatively isolated from the supernatant of the FLK cell culture. For this purpose ultrafiltration through PM-30 membrane, thrice-repeated isoelectric focusing with different (pH 3.0-10.0, pH 4.0-6.0) ampholine intervals and affinity chromatography with ConA-sepharose are used. The SDS-polyacrylamide gel electrophoresis has determined it to be a homogeneous protein with molecular weight 51,000 daltons. The results of the enzyme-linked immunosorbent assay, immunoelectrophoresis and agar-gel immunodiffusion test confirm the specific activity of isolated gp-51 antigen. The gp-51 antigen may be used for identification of antibodies in the blood serum of leukemia virus of infected cattle and for monoclonal screening of antibodies.
在去除与牛白血病病毒不相关的病毒部分后,已从FLK细胞培养物的上清液中制备性分离出(游离的)糖蛋白gp - 51抗原。为此,使用了通过PM - 30膜的超滤、在不同(pH 3.0 - 10.0,pH 4.0 - 6.0)两性电解质间隔下进行三次重复的等电聚焦以及用伴刀豆球蛋白A - 琼脂糖进行亲和层析。SDS - 聚丙烯酰胺凝胶电泳确定其为分子量51,000道尔顿的单一蛋白质。酶联免疫吸附测定、免疫电泳和琼脂凝胶免疫扩散试验的结果证实了分离出的gp - 51抗原的特异性活性。gp - 51抗原可用于鉴定感染牛白血病病毒的血清中的抗体以及用于抗体的单克隆筛选。