Yokota M, Nakamura K, Sugawara K, Homma M
Virology. 1983 Oct 15;130(1):105-17. doi: 10.1016/0042-6822(83)90121-6.
The synthesis of virus-specific polypeptides was analyzed in MDCK cells infected with the JJ/50 strain of influenza C virus. In addition to three major structural proteins gp88, NP, and M, the synthesis of five polypeptides with molecular weights of 29,500 (C1), 27,500 (C2), 24,000 (C3), 19,000 (C4), and 14,000 (C5) was found in infected cells. None of these polypeptides were detected either in virions or in immunoprecipitates obtained after treatment of infected cell lysates with antiviral serum, suggesting that they are not viral structural proteins. Polypeptides C1-C5 were found to be synthesized in MDCK cells infected with different influenza C virus strains as well as in different host cell types infected with C/JJ/50. Further, it was observed that cellular protein synthesis was greatly reduced under hypertonic conditions, whereas the synthesis of C1-C5 was relatively unaffected. These results suggest that polypeptides C1-C5 are virus coded rather than host cell coded. Peptide mapping studies showed that each of polypeptides C3, C4, and C5 had a peptide composition similar to the M protein. The amount of C2 synthesized in infected cells was insufficient for mapping. This polypeptide was, however, found to rapidly disappear in pulse-chase experiments, suggesting that C2 is probably not unique but biosynthetically related to one of the other proteins. In contrast to these polypeptides, polypeptide C1 showed a map which is largely different from any major structural polypeptide. It therefore appears likely that C1 is a nonstructural protein of influenza C virus similar to the NS1 protein of influenza A and B viruses.
对感染C型流感病毒JJ/50株的MDCK细胞中病毒特异性多肽的合成进行了分析。除了三种主要结构蛋白gp88、NP和M外,在感染细胞中还发现了分子量分别为29,500(C1)、27,500(C2)、24,000(C3)、19,000(C4)和14,000(C5)的五种多肽。在病毒粒子中或用抗病毒血清处理感染细胞裂解物后获得的免疫沉淀物中均未检测到这些多肽中的任何一种,这表明它们不是病毒结构蛋白。发现多肽C1 - C5在感染不同C型流感病毒株的MDCK细胞以及感染C/JJ/50的不同宿主细胞类型中均有合成。此外,观察到在高渗条件下细胞蛋白质合成大大减少,而C1 - C5的合成相对不受影响。这些结果表明多肽C1 - C5是病毒编码而非宿主细胞编码的。肽图谱研究表明,多肽C3、C4和C5中的每一种都具有与M蛋白相似的肽组成。在感染细胞中合成的C2量不足以进行图谱分析。然而,在脉冲追踪实验中发现该多肽迅速消失,这表明C2可能不是独特的,但在生物合成上与其他一种蛋白质相关。与这些多肽不同,多肽C1显示出与任何主要结构多肽有很大不同的图谱。因此,C1似乎很可能是C型流感病毒的一种非结构蛋白,类似于A型和B型流感病毒的NS1蛋白。