Tjian R, Robbins A
Proc Natl Acad Sci U S A. 1979 Feb;76(2):610-4. doi: 10.1073/pnas.76.2.610.
A protein antigenically related to the simian virus (SV 40) A gene product has been purified to near homogeneity from cells infected with the adenovirus-SV 40 hybrid virus Ad2(+)D2 and shown to contain ATPase (ATP phosphohydrolase, EC 3.6.1.3) and protein kinase (ATP:phosphotransferase, EC 2.7.1.37) activity. Both enzymatic activities copurify with the protein through six stages including one gel filtration column, two ion exchange columns, and a heparin affinity column. Analogous fractions from extracts of cells uninfected or infected with adenovirus 2 alone do not contain these enzymatic activities. The D2 hybrid protein resolves into two forms (I and II) during ion exchange chromatography. Form I, the major species (85%) of the D2 hybrid protein, elutes from DEAE-Sephadex in 0.37 M NaCl and is able to catalyze the hydrolysis of ATP to ADP + P(i) at a rate of 3 mumol/hr per mg. The remaining 10-15% of the D2 hybrid protein consists of form II which elutes from DEAE-Sephadex in 0.29 M NaCl and is able to hydrolyze ATP as well as to incorporate phosphorus from ATP into either the D2 hybrid protein itself or other protein acceptors such as phosvitin. Although both forms are able to bind DNA, the ATPase activity of form I cosediments with SV 40 DNA more efficiently than does the protein kinase activity of form II during glycerol gradient centrifugation. The ATPase activity of form I is efficiently inhibited by addition of anti-T gamma globulin to the reaction mixture whereas control gamma globulin has no effect. Similarly, the phosphorylation of the D2 hybrid protein by form II is inhibited by anti-T gamma globulin. By contrast, phosphorylation of phosvitin is specifically inhibited by antibody only when the immune complex is removed from the reaction mixture. Thus, it appears likely that one and possibly two enzymatic activities are carried out by the D2 hybrid protein. These findings are discussed in terms of mechanisms of SV 40 DNA replication and virally induced transformation.
一种与猿猴病毒(SV 40)A基因产物抗原相关的蛋白质已从感染腺病毒 - SV 40杂交病毒Ad2(+)D2的细胞中纯化至接近均一,并显示具有ATP酶(ATP磷酸水解酶,EC 3.6.1.3)和蛋白激酶(ATP:磷酸转移酶,EC 2.7.1.37)活性。这两种酶活性与该蛋白质一起通过六个阶段共纯化,包括一个凝胶过滤柱、两个离子交换柱和一个肝素亲和柱。来自未感染或仅感染腺病毒2的细胞提取物的类似级分不含有这些酶活性。D2杂交蛋白在离子交换色谱过程中可分离为两种形式(I和II)。形式I是D2杂交蛋白的主要形式(85%),在0.37 M NaCl中从DEAE - 葡聚糖凝胶上洗脱,能够以每毫克每小时3 μmol的速率催化ATP水解为ADP + P(i)。D2杂交蛋白其余的10 - 15%由形式II组成,它在0.29 M NaCl中从DEAE - 葡聚糖凝胶上洗脱,能够水解ATP并将ATP中的磷掺入D2杂交蛋白本身或其他蛋白质受体如卵黄高磷蛋白中。虽然两种形式都能够结合DNA,但在甘油梯度离心过程中,形式I的ATP酶活性比形式II的蛋白激酶活性更有效地与SV 40 DNA共沉降。通过向反应混合物中添加抗Tγ球蛋白可有效抑制形式I的ATP酶活性,而对照γ球蛋白则无作用。同样,形式II对D2杂交蛋白的磷酸化作用也受到抗Tγ球蛋白的抑制。相比之下,仅当免疫复合物从反应混合物中去除时,抗体才特异性抑制卵黄高磷蛋白的磷酸化。因此,似乎D2杂交蛋白可能执行一种甚至两种酶活性。根据SV 40 DNA复制和病毒诱导转化的机制对这些发现进行了讨论。