Zinoviev V V, Tchikaev N A, Malygin E G
Institute of Molecular Biology, Koltsovo, Russia.
Gene. 1994 Sep 30;147(2):209-14. doi: 10.1016/0378-1119(94)90067-1.
The major envelope protein, p35, of vaccinia virus (VV; strain LIVP) was purified by extraction from virions with the non-ionic detergent Nonidet P-40. The protein was cleaved with CNBr. Four homogeneous peptides were isolated and their N-terminal amino-acid (aa) sequences determined. A computer search of a protein sequence databank revealed complete identity of the determined sequences with aa 44-63, 144-149, 154-165 and 224-238 of ORF H3 of the HindIII-H fragment of the VV genome [Rosel et al., J. Virol. 60 (1989) 436-446]. Earlier, Gordon et al. [Virology 167 (1988) 361-369] determined that the p35 surface protein of VV strain IHD-W is encoded by the H6 gene. Muravlev et al. [Biopolymery i kletka 6 (1990) 83-89 (Russian)] deduced from their data that gene A2 encodes this prominent antigen. Taking into account this ambiguity, we cloned the genes H3, H6 and A2 in expression vectors, prepared the specific antisera against the expression products and conducted the immunochemical analysis of the recombinant and native VV-specific proteins. It has been established that the H6 codes for an early protein that is found only in the infected cell extracts, but is absent in mature virions. The immunodominant protein p35 of VV strain LIVP is encoded by the gene H3. The gene A2 protein product is present mainly in the infected cell extract, but the antiserum against the A2 product shows a rather weak interaction with the 35-kDa fraction of structural VV proteins resolved by electrophoresis.
痘苗病毒(VV;LIVP株)的主要包膜蛋白p35通过用非离子去污剂Nonidet P - 40从病毒粒子中提取进行纯化。该蛋白用溴化氰裂解。分离出四个均一的肽段并测定了它们的N端氨基酸序列。对蛋白质序列数据库进行计算机检索发现,所测定的序列与VV基因组HindIII - H片段的ORF H3的第44 - 63、144 - 149、154 - 165和224 - 238位氨基酸完全相同[Rosel等人,《病毒学杂志》60 (1989) 436 - 446]。早些时候,Gordon等人[《病毒学》167 (1988) 361 - 369]确定VV株IHD - W的p35表面蛋白由H6基因编码。Muravlev等人[《生物聚合物与细胞》6 (1990) 83 - 89(俄语)]根据他们的数据推断基因A2编码这种主要抗原。考虑到这种不确定性,我们将基因H3、H6和A2克隆到表达载体中,制备了针对表达产物的特异性抗血清,并对重组和天然VV特异性蛋白进行了免疫化学分析。已确定H6编码一种仅在感染细胞提取物中发现的早期蛋白,而在成熟病毒粒子中不存在。VV株LIVP的免疫显性蛋白p35由基因H3编码。基因A2的蛋白产物主要存在于感染细胞提取物中,但针对A2产物的抗血清与通过电泳分离的VV结构蛋白的35 kDa部分显示出相当弱的相互作用。