Teramoto Y A, Kufe D, Schlom J
J Virol. 1977 Nov;24(2):525-33. doi: 10.1128/JVI.24.2.525-533.1977.
We recently showed that the 52,000-dalton external glycoprotein (gp52) of the highly oncogenic mouse mammary tumor viruses (MMTVs) of RIII, GR, and C3H mice contains both type- and group-specific antigenic determinants. This was demonstrated by using a competition radioimmunoassay with 125I-externally labeled virions and antisera to the gp52 of MMTV from RIII mice (Proc. Natl. Acad. Sci. U.S.A. 74:3564-3568, 1977). We report here that we were able to distinguish between the gp52's of the high-oncogenic MMTV of C3H mice [MMTV(C3H)] and the low-oncogenic MMTV of that same mouse strain [MMTV(C3Hf)]. This was accomplished by use of a competition radioimmunoassay with 125I-externally labeled virions of MMTV(C3H) and antisera prepared against MMTV(C3H). A comparison of the intact virion and purified gp52 radioimmunoassays showed that MMTV type-specific differences were enhanced with the intact virion radioimmunoassay. These differences were further magnified with appropriately absorbed antisera. These findings thus allow an immunological distinction between the surface glycoproteins of a low-oncogenic endogenous and a high-oncogenic exogenous MMTV of the same mouse strain.
我们最近发现,RIII、GR和C3H小鼠的高度致癌性小鼠乳腺肿瘤病毒(MMTV)的52,000道尔顿外部糖蛋白(gp52)含有型特异性和组特异性抗原决定簇。这是通过使用与125I外部标记的病毒粒子和针对RIII小鼠MMTV的gp52的抗血清进行竞争放射免疫测定来证明的(《美国国家科学院院刊》74:3564 - 3568,1977年)。我们在此报告,我们能够区分C3H小鼠的高致癌性MMTV [MMTV(C3H)]和同一小鼠品系的低致癌性MMTV [MMTV(C3Hf)]的gp52。这是通过使用与MMTV(C3H)的125I外部标记的病毒粒子和针对MMTV(C3H)制备的抗血清进行竞争放射免疫测定来完成的。完整病毒粒子和纯化的gp52放射免疫测定的比较表明,完整病毒粒子放射免疫测定增强了MMTV型特异性差异。用适当吸收的抗血清进一步放大了这些差异。因此,这些发现允许在同一小鼠品系的低致癌性内源性和高致癌性外源性MMTV的表面糖蛋白之间进行免疫学区分。