Oberg B, Saborio J, Persson T, Everitt E, Philipson L
J Virol. 1975 Jan;15(1):199-207. doi: 10.1128/JVI.15.1.199-207.1975.
Adenovirus type 2 mRNA was translated in S30 extracts from Ehrlich ascites and wheat embryo cells. The in vitro products were identified by sodium dodecyl sulfate-gel electrophoresis after immunoprecipitation with specific antisera in the presence of urea. Seven virion polypeptides could be identified by immunoprecipitation. Three of these appear to be precursors to polypeptides of the virion. mRNA isolated late in adenovirus infection was separated into three size classes by zonal sedimentation. Material sedimenting at 26S was translated into polypeptides corresponding to the largest virion polypeptides II to IV, a 22S fraction corresponding to polypeptide V, and smaller polypeptides and a 15S fraction corresponding to polypeptide IX. A significant amount of polypeptide IX was also synthesized by the 26S and 22S RNA.
2型腺病毒mRNA在艾氏腹水细胞和小麦胚细胞的S30提取物中进行翻译。在尿素存在的情况下,用特异性抗血清进行免疫沉淀后,通过十二烷基硫酸钠-凝胶电泳鉴定体外产物。通过免疫沉淀可鉴定出七种病毒粒子多肽。其中三种似乎是病毒粒子多肽的前体。在腺病毒感染后期分离的mRNA通过区带沉降分为三个大小类别。沉降在26S的物质被翻译成对应于最大病毒粒子多肽II至IV的多肽,22S部分对应于多肽V,较小的多肽和15S部分对应于多肽IX。26S和22S RNA也合成了大量的多肽IX。