Höss A, Moarefi I, Scheidtmann K H, Cisek L J, Corden J L, Dornreiter I, Arthur A K, Fanning E
Institute for Biochemistry, Munich, Federal Republic of Germany.
J Virol. 1990 Oct;64(10):4799-807. doi: 10.1128/JVI.64.10.4799-4807.1990.
The phosphorylation pattern of simian virus 40 (SV40) large tumor (T) antigen purified from insect cells infected with a recombinant baculovirus was compared with that reported previously for T antigen from SV40-infected monkey cells. The specific activity of metabolic phosphate labeling of baculovirus T antigen was reduced, and the phosphopeptide map of the baculovirus protein, while qualitatively similar to that of lytic T, revealed several quantitative differences. The most striking difference was the prominence in the baculovirus map of peptides containing phosphothreonine 124. These peptides are known to arise from other phosphopeptides upon dephosphorylation of neighboring serines, suggesting that baculovirus T may be underphosphorylated at these serines and perhaps other sites. Functional assays used to further investigate the phosphorylation state of the baculovirus protein included SV40 DNA binding after enzymatic dephosphorylation with alkaline phosphatase and after phosphorylation by a murine homolog of cdc2 protein kinase. The results imply that baculovirus T antigen is underphosphorylated, in particular at those serine residues whose phosphorylation is responsible for down regulation of DNA-binding activity at site II in the core origin of DNA replication. In contrast, no evidence for a functionally significant underphosphorylation at threonine 124 could be found.
将从感染重组杆状病毒的昆虫细胞中纯化的猴病毒40(SV40)大T抗原的磷酸化模式,与先前报道的来自SV40感染猴细胞的T抗原的磷酸化模式进行了比较。杆状病毒T抗原的代谢磷酸盐标记比活性降低,并且杆状病毒蛋白的磷酸肽图谱虽然在定性上与裂解T抗原的图谱相似,但显示出一些定量差异。最显著的差异是在杆状病毒图谱中含有磷酸苏氨酸124的肽段很突出。已知这些肽段是在相邻丝氨酸去磷酸化后从其他磷酸肽产生的,这表明杆状病毒T抗原在这些丝氨酸以及可能的其他位点可能磷酸化不足。用于进一步研究杆状病毒蛋白磷酸化状态的功能测定包括用碱性磷酸酶进行酶促去磷酸化后以及用cdc2蛋白激酶的鼠同源物进行磷酸化后进行的SV40 DNA结合测定。结果表明杆状病毒T抗原磷酸化不足,特别是在那些其磷酸化负责下调DNA复制核心起始位点II处DNA结合活性的丝氨酸残基处。相比之下,未发现苏氨酸124处存在功能上显著的磷酸化不足的证据。