Hopkins N, Schindler J, Hynes R
J Virol. 1977 Jan;21(1):309-18. doi: 10.1128/JVI.21.1.309-318.1977.
We have examined the electrophoretic mobility on sodium dodecyl sulfate-polyacrylamide gels of three virion proteins of B-tropic murine leukemia virus from BALB/c and six of its NB-tropic derivatives. The gp70 protein and a 13,000-molecular-weight virion protein tentatively identified as p15 of the NB-tropic viruses migrated with the corresponding B virus proteins. However, the major internal structural protein of type C virions, p30, of all the NB-tropic viruses migrated more rapidly than the p30 of their B virus progenitor. Although this change in p30 raises the possibility that p30 may be involved in determining the N-, B-, or NB-tropism of MuLV's, it is also possible that the change accompanies but does not directly determine the change in tropsim.
我们检测了来自BALB/c的B嗜性鼠白血病病毒的三种病毒体蛋白及其六种NB嗜性衍生物在十二烷基硫酸钠-聚丙烯酰胺凝胶上的电泳迁移率。gp70蛋白和一种分子量为13000的病毒体蛋白(初步鉴定为NB嗜性病毒的p15)与相应的B病毒蛋白一起迁移。然而,所有NB嗜性病毒的C型病毒体的主要内部结构蛋白p30,比其B病毒亲本的p30迁移得更快。尽管p30的这种变化增加了p30可能参与决定鼠白血病病毒的N嗜性、B嗜性或NB嗜性的可能性,但也有可能这种变化伴随但不直接决定嗜性的改变。