Kress M, May E, Cassingena R, May P
J Virol. 1979 Aug;31(2):472-83. doi: 10.1128/JVI.31.2.472-483.1979.
In addition to the virus-coded large-T and small-t antigens, two new classes of proteins were immunoprecipitated by anti-simian virus 40 (SV40) tumor serum from extracts of various SV40-transformed cell lines. These were as follows: (i) proteins (termed "super-T proteins") with an Mr higher than that of large-T antigen (86,000), which were found in many SV40-transformed cell lines derived from mouse and rat cells (super-T proteins and large-T antigen appeared to have closely related structures as judged by the Chromobead elution patterns of their methionine-labeled tryptic peptides); (ii) proteins (termed "55K proteins") with an Mr ranging from 50,000 to 60,000, which were present in all SV40-transformed cell lines examined so far, including those obtained by chromosome-mediated gene transfer. The 55K proteins were not structurally related to large-T antigens, as judged by the Chromobead elution patterns of their methionine-labeled tryptic peptides. Our data are compatible with the assumption that the 55K proteins are largely or totally cell coded.
除了病毒编码的大T和小t抗原外,用抗猴病毒40(SV40)肿瘤血清从各种SV40转化细胞系的提取物中免疫沉淀出两类新的蛋白质。具体如下:(i)分子量高于大T抗原(86,000)的蛋白质(称为“超级T蛋白”),在许多源自小鼠和大鼠细胞的SV40转化细胞系中发现(根据其甲硫氨酸标记的胰蛋白酶肽的Chromobead洗脱模式判断,超级T蛋白和大T抗原似乎具有密切相关的结构);(ii)分子量在50,000至60,000之间的蛋白质(称为“55K蛋白”),在迄今检测的所有SV40转化细胞系中都存在,包括通过染色体介导的基因转移获得的细胞系。根据其甲硫氨酸标记的胰蛋白酶肽的Chromobead洗脱模式判断,55K蛋白与大T抗原在结构上不相关。我们的数据与55K蛋白主要或完全由细胞编码的假设相符。