Ito H, Minamoto N, Goto H, Rong L T, Sugiyama M, Kinjo T
Department of Veterinary Public Health, Faculty of Agriculture, Gifu University, Japan.
Vet Microbiol. 1996 Apr;49(3-4):257-65. doi: 10.1016/0378-1135(95)00193-x.
A gene encoding the major inner capsid protein, VP6, of avian rotavirus was inserted into the eukaryotic expression vector pAX-91 under the control of the SR alpha promoter and was expressed at a high level in simian COS7 cells. The expressed VP6 was indistinguishable in terms of electrophoretic mobility from the corresponding protein synthesized in simian MA104 cells infected with avian rotavirus. Binding assays with a series of monoclonal antibodies (mAbs) that corresponded to four antigenic sites on VP6 of avian rotavirus showed that the antigenic characteristics of the expressed product were identical to those of the native VP6 of avian rotavirus virions. Fiber-like structures that reacted strongly with antiserum against rotavirus were observed in VP6-expressing COS7 cells. Furthermore, an analysis of the tertiary structure of the expressed VP6 protein indicated that it adopts a trimeric configuration, similar to that of the major inner capsid protein of PO-13 virus. From these results, it appears that recombinant VP6 will facilitate studies of the structure and function of authentic VP6, an important protein in avian rotavirus.
将编码禽轮状病毒主要内衣壳蛋白VP6的基因插入到真核表达载体pAX - 91中,该载体受SRα启动子控制,并在猴COS7细胞中高水平表达。所表达的VP6在电泳迁移率方面与感染禽轮状病毒的猴MA104细胞中合成的相应蛋白没有区别。用一系列对应于禽轮状病毒VP6上四个抗原位点的单克隆抗体(mAb)进行结合试验表明,表达产物的抗原特性与禽轮状病毒颗粒天然VP6的抗原特性相同。在表达VP6的COS7细胞中观察到与抗轮状病毒抗血清强烈反应的纤维状结构。此外,对所表达的VP6蛋白三级结构的分析表明,它采用三聚体构型,类似于PO - 13病毒的主要内衣壳蛋白。从这些结果来看,重组VP6将有助于对禽轮状病毒中重要蛋白——天然VP6的结构和功能进行研究。