Wong T C, Hirano A
J Virol. 1986 Jan;57(1):343-8. doi: 10.1128/JVI.57.1.343-348.1986.
A cDNA library designed for high-level expression of measles virus-specific gene products in mammalian cells was generated. From this library, functional clones which contained the entire protein-coding sequences of the nucleocapsid (N) and the phosphoprotein (P) genes were isolated. By DNA-mediated gene transfer into a line of simian virus 40-transformed monkey kidney cells, the N-specific cDNA was expressed into a single polypeptide of about 60,000 Mr, which was immunoprecipitated by monoclonal antibodies against the measles virus N protein. In contrast, the P-specific cDNA could be expressed into either one or two species of polypeptides of 75,000 or 70,000 Mr, both of which were immunoprecipitated by monoclonal antibodies against the measles virus P protein.
构建了一个用于在哺乳动物细胞中高水平表达麻疹病毒特异性基因产物的cDNA文库。从该文库中分离出了包含核衣壳(N)蛋白和磷蛋白(P)基因完整蛋白质编码序列的功能克隆。通过DNA介导的基因转移,将N特异性cDNA导入一株经猿猴病毒40转化的猴肾细胞系,表达出一条约60,000 Mr的单一多肽,该多肽可被抗麻疹病毒N蛋白的单克隆抗体免疫沉淀。相比之下,P特异性cDNA可表达为75,000或70,000 Mr的一种或两种多肽,这两种多肽均可被抗麻疹病毒P蛋白的单克隆抗体免疫沉淀。