Griffin J D, Light S, Livingston D M
J Virol. 1978 Jul;27(1):218-26. doi: 10.1128/JVI.27.1.218-226.1978.
A measure of the molecular weight of the large simian virus 40 T antigen was sought by SDS-polyacrylamide gel electrophoresis, random-coil chromatography, and sedimentation-velocity analysis in a density gradient. Large T antigen obtained from a simian virus 40-transformed human cell line either by immunoprecipitation or by standard preparatory methods migrated like a 94,000-molecular-weight (approximately 94K) polypeptide in SDS-gels but was found to have an approximate was observed with T antigen obtained from lytically infected monkey cells. In view of the strong theoretical basis for the guanidine method and the agreement with the sedimentation data, these findings suggest that the molecular weight of this protein is approximately 75 to 80K as opposed to 94 to 100K and, therefore, that considerably less than the entire early region of simian virus 40 is required to encode it. This size estimate is in keeping with earlier results which revealed a normal-size T antigen in cells infected with viable deletion mutants lacking as much as 10% of the early region.
通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳、无规卷曲色谱法以及密度梯度沉降速度分析,来探寻大猿猴病毒40 T抗原的分子量。从猿猴病毒40转化的人细胞系中通过免疫沉淀或标准制备方法获得的大T抗原,在十二烷基硫酸钠凝胶中迁移时表现得像一种分子量为94,000(约94K)的多肽,但发现其分子量约为[此处原文缺失具体数值],这与从裂解感染的猴细胞中获得的T抗原情况相同。鉴于胍法有坚实的理论基础且与沉降数据相符,这些发现表明该蛋白的分子量约为75至80K,而非94至100K,因此,编码它所需的猿猴病毒40早期区域远少于整个早期区域。这一大小估计与早期结果一致,早期结果显示,在感染了缺失多达10%早期区域的存活缺失突变体的细胞中存在正常大小的T抗原。