Kennel S J, Tennant R W
J Virol. 1979 Jun;30(3):729-34. doi: 10.1128/JVI.30.3.729-734.1979.
Murine sarcoma virus pseudotypes were prepared by infection of nonproducer cells (A1-2), which were transformed by the Gazdar strain of mouse sarcoma virus, with Gross (N-tropic), WN1802B (B-tropic), or Moloney (NB-tropic) viruses. The respective host range pseudotype sarcoma viruses were defined by the titration characteristics on cells with the appropriate Fv-1 genotype. Proteins from virus progeny were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Bands present in both the 65,000- and the 10,000- to 20,000- molecular-weight regions of the gel distinguished the pseudotype viruses from their respective helpers. Furthermore, two protein bands were noted in the p30 region of murine sarcoma virus (Gross), one corresponding to Gross virus p30, and another of slightly slower mobility. However, since the mobility of the putative sarcoma p30 is nearly indentical to that of WN1802B, its presence could not be established by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Type-specific radioimmunoassays for Gross virus p30 and for WN1802B p30 were applied for analysis of pseudotype preparations, and among several ecotropic viruses tested, only the homologous virus scored in the respective assay. By use of these assays, pseudotype viruses were found to contain only 8 to 48% helper-specific p30's; the remainder is presumably derived from the sarcoma virus.
通过用格罗斯(N-嗜性)、WN1802B(B-嗜性)或莫洛尼(NB-嗜性)病毒感染由小鼠肉瘤病毒加兹达毒株转化的非生产性细胞(A1-2)来制备鼠肉瘤病毒假型。各自的宿主范围假型肉瘤病毒通过在具有适当Fv-1基因型的细胞上的滴定特性来定义。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析病毒子代的蛋白质。凝胶中分子量在65,000以及10,000至20,000区域出现的条带将假型病毒与其各自的辅助病毒区分开来。此外,在鼠肉瘤病毒(格罗斯)的p30区域注意到两条蛋白带,一条对应于格罗斯病毒p30,另一条迁移率稍慢。然而,由于假定的肉瘤p30的迁移率与WN1802B几乎相同,因此无法通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳确定其存在。应用针对格罗斯病毒p30和WN1802B p30的型特异性放射免疫测定法分析假型制剂,在所测试的几种亲嗜性病毒中,只有同源病毒在各自的测定中得分。通过使用这些测定法,发现假型病毒仅含有8%至48%的辅助病毒特异性p30;其余部分大概来自肉瘤病毒。