Oskarsson M K, Robey W G, Harris C L, Fischinger P J, Haapala D K, Vande Woude G F
Proc Natl Acad Sci U S A. 1975 Jun;72(6):2380-4. doi: 10.1073/pnas.72.6.2380.
A 60,000-dalton polypeptide (p60) has been identified in the feline leukemia virus (FeLV) pseudotype of Moloney sarcoma virus [MSV(FeLV)]. This polypeptide is present in the purified virus complex in concentrations greater than either the murine p30 or the feline p27. Purified p60 crossreacts immunologically with murine p30 group antiserum and contains several interspecies determinants, whereas the group specific determinant of FeLV p27 is not detected. Comparison of peptide fingerprints of p60 and murine p30 show many peptides in common. Limited digestion of p60 with either trypsin or chymotrypsin produced p30-35 and p20 peptides which retain the MuLV p30 group and interspecies antigenic activities. The p30 produced by both enzymes comigrates in polyacrylamide gels with the murine p30 of MSV(FeLV), thus suggesting that p60 may be an uncleaved precursor to p30.
在莫洛尼肉瘤病毒的猫白血病病毒(FeLV)假型[MSV(FeLV)]中已鉴定出一种60,000道尔顿的多肽(p60)。这种多肽在纯化的病毒复合物中的浓度高于鼠源p30或猫源p27。纯化的p60与鼠源p30组抗血清发生免疫交叉反应,并含有几种种间决定簇,而未检测到FeLV p27的组特异性决定簇。p60和鼠源p30的肽指纹图谱比较显示有许多共同的肽段。用胰蛋白酶或糜蛋白酶对p60进行有限消化产生了保留MuLV p30组和种间抗原活性的p30 - 35和p20肽段。两种酶产生的p30在聚丙烯酰胺凝胶中与MSV(FeLV)的鼠源p30迁移率相同,因此表明p60可能是p30的未切割前体。