Hongo S, Gao P, Sugawara K, Muraki Y, Matsuzaki Y, Tada Y, Kitame F, Nakamura K
Department of Bacteriology, Yamagata University, School of Medicine, Japan.
J Gen Virol. 1998 Sep;79 ( Pt 9):2207-13. doi: 10.1099/0022-1317-79-9-2207.
Unspliced mRNA from RNA segment 6 of influenza C virus contains a single open reading frame that potentially encodes a polypeptide of 374 amino acids. This polypeptide, which has not been identified as yet, is predicted to contain the complete amino acid sequence of the matrix protein, M1, as well as that of a small integral membrane protein, CM2. Here, we found that small amounts of two previously unrecognized proteins with apparent molecular masses of 42 (P42) and 44 kDa (P44) were immunoprecipitated with immune serum against CM2. The electrophoretic mobilities of P42 and P44 varied depending on virus strain, indicating that they are virus-coded. Treatment of infected cells with tunicamycin and digestion of immunoprecipitated proteins with various endoglycosidases revealed that P42 is modified by the addition of a high-mannose oligosaccharide chain to generate P44. A monoclonal antibody against M1, like anti-CM2 serum, was able to immunoprecipitate both the P42 and P44 proteins. Furthermore, the tryptic peptide map of either P42 or P44 was indistinguishable from the map of the mixture of M1 and CM2. These results, taken together, suggest strongly that P42 and P44 correspond to the 374 amino acid protein encoded by unspliced RNA segment 6 mRNA and its N-glycosylated form, respectively.
丙型流感病毒RNA片段6的未剪接mRNA含有一个单一的开放阅读框,可能编码一个由374个氨基酸组成的多肽。该多肽尚未被鉴定出来,预计包含基质蛋白M1以及小整合膜蛋白CM2的完整氨基酸序列。在这里,我们发现用抗CM2免疫血清免疫沉淀出少量两种先前未被识别的蛋白质,其表观分子量分别为42 kDa(P42)和44 kDa(P44)。P42和P44的电泳迁移率因病毒株而异,表明它们是病毒编码的。用衣霉素处理感染细胞并用各种内切糖苷酶消化免疫沉淀的蛋白质,结果显示P42通过添加高甘露糖寡糖链进行修饰从而产生P44。与抗CM2血清一样,抗M1单克隆抗体能够免疫沉淀P42和P44蛋白。此外,P42或P44的胰蛋白酶肽图与M1和CM2混合物的肽图无法区分。综上所述,这些结果强烈表明P42和P44分别对应于未剪接的RNA片段6 mRNA编码的374个氨基酸蛋白及其N-糖基化形式。