Ballmer-Hofer K, Benjamin T L
EMBO J. 1985 Sep;4(9):2321-7. doi: 10.1002/j.1460-2075.1985.tb03933.x.
We have studied phosphorylation carried out by purified plasma membranes from polyoma virus-infected cells. When isolated membranes are incubated with [gamma-32P]ATP, polyoma virus middle T antigen (mT) becomes phosphorylated on tyrosine. Partial proteolysis mapping shows the same pattern as previously noted for mT labeled in immune complexes. Membranes labeled in vitro were also extracted and immunoprecipitated with anti-T or anti-src antibody. With either antibody, both mT and pp60c-src were brought down and shown to be labeled on tyrosine. The mT of an hr-t mutant (NG59) showed only a trace amount of labeling in membranes under the same conditions. Proteins from infected and uninfected cell membranes labeled in vitro were separated on two-dimensional gels. An acidic 40-kd phosphoprotein was labeled in uninfected cell membranes, but was not seen using membranes from wild-type virus-infected cells. Neither NG59, which encodes a defective but membrane-associated mT, nor a mutant encoding a truncated mT that fails to associate with membranes, alters the level of the 40-kd phosphoprotein in membranes labeled in vitro. These results suggest that mT, acting through pp60c-src and possibly other cellular kinases and phosphatases, can affect cell protein phosphorylation as part of the transformation process.
我们研究了从多瘤病毒感染细胞中纯化的质膜所进行的磷酸化作用。当分离的膜与[γ-32P]ATP一起温育时,多瘤病毒中T抗原(mT)在酪氨酸上发生磷酸化。部分蛋白酶解图谱显示出与先前在免疫复合物中标记的mT所观察到的相同模式。体外标记的膜也被提取并用抗T或抗src抗体进行免疫沉淀。使用任何一种抗体,mT和pp60c-src都被沉淀下来并显示在酪氨酸上被标记。在相同条件下,hr-t突变体(NG59)的mT在膜中仅显示出微量的标记。将体外标记的感染和未感染细胞膜中的蛋白质在二维凝胶上分离。一种酸性的40-kd磷蛋白在未感染的细胞膜中被标记,但在野生型病毒感染细胞的膜中未观察到。编码有缺陷但与膜相关的mT的NG59,以及编码截短的mT且不能与膜结合的突变体,都不会改变体外标记的膜中40-kd磷蛋白的水平。这些结果表明,mT通过pp60c-src以及可能的其他细胞激酶和磷酸酶发挥作用,作为转化过程的一部分,可以影响细胞蛋白质磷酸化。