Baines J D, Roizman B
Marjorie B. Kovler Viral Oncology Laboratories, University of Chicago, Illinois 60637.
J Virol. 1993 Mar;67(3):1441-52. doi: 10.1128/JVI.67.3.1441-1452.1993.
The herpes simplex virus 1 UL10 gene encodes a hydrophobic membrane protein dispensable for viral replication in cell culture (J.D. Baines and B. Roizman, J. Virol. 65:938-944, 1991). We report the following. (i) A fusion protein consisting of glutathione S-transferase fused to the C-terminal 93 amino acids of the UL10 protein was used to produce a rabbit polyclonal antiserum. The antiserum reacted with infected-cell proteins which formed in denaturing polyacrylamide gels a sharp band (apparent M(r) of 50,000) and a very broad band (M(r) of 53,000 to 63,000). These bands were not formed by lysates of UL10- virus or by lysates of infected cells boiled in the presence of sodium dodecyl sulfate before electrophoresis. (ii) The proteins forming both bands were labeled by [3H]glucosamine, indicating that they were glycosylated. (iii) The UL10 protein in cells treated with tunicamycin formed a single band (apparent M(r) of 47,000) reactive with the anti-UL10 antibody, indicating that the 47,000-M(r) protein was a precursor of N-glycosylated, more slowly migrating forms of UL10. Treatment of the immunoprecipitate with endoglycosidase H increased the electrophoretic mobility of the 50,000-M(r) species to that of the 47,000-M(r) species, indicating that the 50,000-M(r) species contained high-mannose polysaccharide chains, whereas the proteins forming the 53,000- to 63,000-M(r) bands contained mature chains inasmuch as they were resistant to digestion by the enzyme. (iv) The UL10 protein of R7221 carrying a 20-amino-acid epitope formed only one band with an M(r) of 53,000. This band was sensitive to endoglycosidase H, suggesting that the epitope inserted in the R7221 UL10 protein may have interfered with glycosylation. (v) The UL10 protein does not contain a cleavable signal sequence inasmuch as the first UL10 methionine codon was reflected in the 50,000-M(r) protein. (vi) The UL10 protein is present in virions and plasma membranes of unfixed cells that were reacted with the polyclonal rabbit antibody. In accordance with the current nomenclature, the UL10 protein is designated glycoprotein M.
单纯疱疹病毒1型UL10基因编码一种疏水膜蛋白,该蛋白在细胞培养中对病毒复制并非必需(J.D. 贝恩斯和B. 罗伊兹曼,《病毒学杂志》65:938 - 944, 1991)。我们报告如下:(i)一种由谷胱甘肽S - 转移酶与UL10蛋白的C末端93个氨基酸融合而成的融合蛋白,用于制备兔多克隆抗血清。该抗血清与感染细胞蛋白发生反应,这些蛋白在变性聚丙烯酰胺凝胶中形成一条清晰的条带(表观分子量为50,000)和一条非常宽的条带(分子量为53,000至63,000)。这些条带不是由UL10 - 病毒的裂解物或在电泳前于十二烷基硫酸钠存在下煮沸的感染细胞裂解物形成的。(ii)形成这两条带的蛋白都被[³H]葡糖胺标记,表明它们被糖基化。(iii)用衣霉素处理的细胞中的UL10蛋白形成一条与抗UL10抗体反应的单一条带(表观分子量为47,000),表明47,000分子量的蛋白是UL10的N - 糖基化、迁移较慢形式的前体。用内切糖苷酶H处理免疫沉淀物后,50,000分子量条带的电泳迁移率增加到47,000分子量条带的迁移率,表明50,000分子量条带含有高甘露糖多糖链,而形成53,000至63,000分子量条带的蛋白含有成熟链,因为它们对该酶的消化具有抗性。(iv)携带20个氨基酸表位的R7221的UL10蛋白仅形成一条分子量为53,000的条带。这条带对内切糖苷酶H敏感,表明插入R7221 UL10蛋白中的表位可能干扰了糖基化。(v)ULl0蛋白不包含可裂解的信号序列,因为50,000分子量蛋白中反映了UL10的第一个甲硫氨酸密码子。(vi)UL10蛋白存在于与兔多克隆抗体反应的未固定细胞的病毒粒子和质膜中。根据当前的命名法,UL10蛋白被命名为糖蛋白M。