Schaffhausen B S, Bockus B J, Berkner K L, Kaplan D, Roberts T M
J Virol. 1987 Apr;61(4):1221-5. doi: 10.1128/JVI.61.4.1221-1225.1987.
The adenovirus Ad5(pymT) has been used to express middle T antigen at very high levels in 293 cells. The middle T antigen produced was localized to membranes and was modified in the same way as that expressed in polyoma virus-infected mouse cells. It was phosphorylated in vivo on serine residues and in vitro on tyrosine residues. The in vivo phosphorylations occurred between residues 223 and 275. The middle T antigen encoded by A d5(pymT) was phosphorylated in vitro in a complex with human pp60c-src. Interestingly, the extreme overexpression of middle T antigen did not cause a parallel increase in the amount of complex; most of the pp60c-src remained unassociated. Immunoaffinity purification resulted in approximately 100 micrograms of middle T antigen from a 100-mm tissue culture dish. Several cell proteins copurified with the Ad5(pymT)-derived middle T antigen. Two of these, the 74- and 63-kilodalton species, are of particular interest because they were also purified from mouse tumors expressing middle T antigen.
腺病毒Ad5(pymT)已被用于在293细胞中高水平表达中T抗原。所产生的中T抗原定位于细胞膜,并且其修饰方式与在多瘤病毒感染的小鼠细胞中表达的中T抗原相同。它在体内丝氨酸残基上被磷酸化,在体外酪氨酸残基上被磷酸化。体内磷酸化发生在223至275位残基之间。Ad5(pymT)编码的中T抗原在体外与人pp60c-src形成复合物时被磷酸化。有趣的是,中T抗原的极度过表达并未导致复合物数量的平行增加;大多数pp60c-src仍未结合。免疫亲和纯化从一个100毫米组织培养皿中得到了约100微克的中T抗原。几种细胞蛋白与源自Ad5(pymT)的中T抗原共同纯化。其中两种,74千道尔顿和63千道尔顿的蛋白特别值得关注,因为它们也从表达中T抗原的小鼠肿瘤中被纯化出来。