Mullarkey M F, Hruska J F, Takemoto K K
J Virol. 1974 May;13(5):1014-9. doi: 10.1128/JVI.13.5.1014-1019.1974.
The proteins of simian virus 40 (SV40) and two human papovaviruses, the hemagglutinating BK virus and the non-hemagglutinating DAR virus, were analyzed and compared by sodium dodecyl sulfate polyacrylamide gel electrophoresis. The virions of SV40 and DAR contain seven proteins. By molecular weight analysis the constituent proteins of SV40 and DAR are identical. Approximately 84% of the viral protein has a molceular weight of 45,000. The major protein of BK virus is 3,000 to 5,000 daltons lighter than the major proteins of SV40 and DAR viruses. The five most rapidly migrating proteins of BK virus are indistinguishable by molecular weight analysis from the corresponding proteins of SV40 and DAR viruses. Radial immunodiffusion and immunoelectrophoresis of whole virus gave lines of identity between SV40 and DAR when reacted with SV40 antibody. SV40 antiserum tested against BK virus and BK antiserum tested against SV40 virus showed no reactivity by complement fixation, immunodiffusion, or immunoelectrophoresis.
通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳对猴病毒40(SV40)以及两种人乳头瘤空泡病毒——血凝性BK病毒和非血凝性DAR病毒的蛋白质进行了分析和比较。SV40和DAR病毒粒子含有七种蛋白质。通过分子量分析,SV40和DAR的组成蛋白是相同的。约84%的病毒蛋白分子量为45,000。BK病毒的主要蛋白比SV40和DAR病毒的主要蛋白轻3,000至5,000道尔顿。通过分子量分析,BK病毒迁移速度最快的五种蛋白与SV40和DAR病毒的相应蛋白无法区分。全病毒的放射免疫扩散和免疫电泳结果显示,当与SV40抗体反应时,SV40和DAR之间呈现同一性条带。用SV40抗血清检测BK病毒,以及用BK抗血清检测SV40病毒,通过补体结合、免疫扩散或免疫电泳均未显示出反应性。