Blackhall J, Fuentes A, Hansen K, Magnusson G
Department of Medical Immunology and Microbiology, Uppsala University, Sweden.
J Virol. 1997 Jan;71(1):138-44. doi: 10.1128/JVI.71.1.138-144.1997.
The rotavirus nonstructural protein NSP5, a product of the smallest genomic RNA segment, is a phosphoprotein containing O-linked N-acetylglucosamine. We investigated the phosphorylation of NSP5 in monkey MA104 cells infected with simian rotavirus SA11. Immunoprecipitated NSP5 was analyzed with respect to phosphorylation and protein kinase activity. After metabolic labeling of NSP5 with 32Pi, only serine residues were phosphorylated. Separation of tryptic peptides revealed four to six strongly labeled products and several weakly labeled products. Phosphorylation at multiple sites was also shown by two-dimensional polyacrylamide gel electrophoresis (PAGE), where several isoforms of NSP5 with different pIs were identified. Analysis by PAGE of protein reacting with an NSP5-specific antiserum showed major forms at 26 to 28 and 35 kDa. Moreover, there were polypeptides migrating between 28 and 35 kDa. Treatment of the immunoprecipitated material with protein phosphatase 2A shifted the mobilities of the 28- to 35-kDa polypeptides to the 26-kDa position, suggesting that the slower electrophoretic mobility was caused by phosphorylation. Radioactive labeling showed that the 26-kDa form contained additional phosphate groups that were not removed by protein phosphatase 2A. The immunoprecipitated NSP5 possessed protein kinase activity. Incubation with [gamma-32P]ATP resulted in 32P labeling of 28- to 35-kDa NSP5. The distribution of 32P radioactivity between the components of the complex was similar to the phosphorylation in vivo. Assays of the protein kinase activity of a glutathione S-transferase-NSP5 fusion polypeptide expressed in Escherichia coli demonstrated autophosphorylation, suggesting that NSP5 was the active component in the material isolated from infected cells.
轮状病毒非结构蛋白NSP5是最小基因组RNA片段的产物,是一种含有O-连接的N-乙酰葡糖胺的磷蛋白。我们研究了感染猿猴轮状病毒SA11的猴MA104细胞中NSP5的磷酸化情况。对免疫沉淀的NSP5进行了磷酸化和蛋白激酶活性分析。用32Pi对NSP5进行代谢标记后,只有丝氨酸残基被磷酸化。胰蛋白酶肽段的分离显示有4至6个强标记产物和几个弱标记产物。二维聚丙烯酰胺凝胶电泳(PAGE)也显示了多个位点的磷酸化,其中鉴定出了几种具有不同pI的NSP5同工型。用NSP特异性抗血清进行PAGE分析,显示主要形式在26至28 kDa和35 kDa。此外,还有在28至35 kDa之间迁移的多肽。用蛋白磷酸酶2A处理免疫沉淀的物质,使28至35 kDa多肽的迁移率移至26 kDa位置,这表明较慢的电泳迁移率是由磷酸化引起的。放射性标记显示,26 kDa形式含有蛋白磷酸酶2A不能去除的额外磷酸基团。免疫沉淀的NSP5具有蛋白激酶活性。与[γ-32P]ATP一起孵育导致28至35 kDa的NSP5被32P标记。复合物各组分之间32P放射性的分布与体内磷酸化情况相似。对在大肠杆菌中表达的谷胱甘肽S-转移酶-NSP5融合多肽的蛋白激酶活性测定表明存在自磷酸化,这表明NSP5是从感染细胞中分离出的物质中的活性成分。