Kosiakova N P, Posevaia T A, Zhdanov V M
Vopr Virusol. 1979 Jul-Aug(4):381-5.
Continuous cells of human origin, HEp-2, and mouse L929 cells taken 24 hours after infection with oncornavirus D were labeled for protein with a mixture of 14C-amino acids and 3H-glucosamine. Specific sera obtained from rabbits were used for testing the virus-specific new antigen in cell extracts and for immunoprecipitation of the new antigen. Electrophoresis in polyacryl amide gel showed the virusspecific new antigen, common for human HEp-2 cells and for oncornavirus-D-infected mouse L929 cells, to be a glycoprotein with a molecular weight of 98,000--100,000 daltons. By its molecular weight it differs from oncornavirus envelope glycoprotein whose molecular weight is 60,000--70,000 daltons. No similar protein was found in noninfected L929 cells.
用人源连续细胞系HEp - 2以及感染了D型肿瘤病毒24小时后的小鼠L929细胞,用¹⁴C - 氨基酸和³H - 葡糖胺的混合物对蛋白质进行标记。从兔子获得的特异性血清用于检测细胞提取物中的病毒特异性新抗原以及对新抗原进行免疫沉淀。聚丙烯酰胺凝胶电泳显示,人HEp - 2细胞和感染D型肿瘤病毒的小鼠L929细胞共有的病毒特异性新抗原是一种分子量为98,000 - 100,000道尔顿的糖蛋白。就分子量而言,它与分子量为60,000 - 70,000道尔顿的肿瘤病毒包膜糖蛋白不同。在未感染的L929细胞中未发现类似蛋白质。