Lamb R A, Zebedee S L, Richardson C D
Cell. 1985 Mar;40(3):627-33. doi: 10.1016/0092-8674(85)90211-9.
The influenza A virus M2 protein is expressed abundantly at the cell surface, and in addition to the hemagglutinin (HA) and neuraminidase (NA), is a third virus-specific membrane protein. M2 has an internal hydrophobic membrane anchorage domain and associates with the same cellular membrane fractions as HA and NA. Trypsin treatment of infected cells and immunoprecipitation with site-specific antisera indicate that a minimum of 18 NH2-terminal amino acids of M2 are exposed at the cell surface. Ten NH2-terminal residues are conserved in all strains of influenza A virus for which sequences are available. Antibodies can recognize M2 on the cell surface and therefore it may be an infected-cell surface antigen. We discuss properties of M2 that match it to the elusive major target molecule on influenza A virus-infected cells for cross-reactive cytotoxic T cells.
甲型流感病毒M2蛋白在细胞表面大量表达,除血凝素(HA)和神经氨酸酶(NA)外,它是第三种病毒特异性膜蛋白。M2具有一个内部疏水膜锚定结构域,并与HA和NA存在于相同的细胞膜组分中。用胰蛋白酶处理感染细胞并用位点特异性抗血清进行免疫沉淀表明,M2至少有18个NH2末端氨基酸暴露在细胞表面。在所有已获得序列的甲型流感病毒毒株中,有10个NH2末端残基是保守的。抗体能够识别细胞表面的M2,因此它可能是一种感染细胞表面抗原。我们讨论了M2的特性,这些特性使其成为甲型流感病毒感染细胞上难以捉摸的主要靶分子,以产生交叉反应性细胞毒性T细胞。