Khan A S, Stephenson J R
J Virol. 1977 Sep;23(3):599-607. doi: 10.1128/JVI.23.3.599-607.1977.
The major non-glycosylated structural proteins of feline leukemia virus have been isolated, and competition immunoassays have been developed for each. These proteins include the 27,000- to 30,000-molecular-weight major internal antigen designated p30, a 15,000-molecular-weight protein (p15), an acidic protein of 12,000 molecular weight (p12), and a highly basic 10,000-molecular-weight protein (p10). Immunologically and biochemically corresponding proteins of feline and murine leukemia viruses have been identified. and, on the basis of analogy to the known sequence of a prototype type C virus of mouse origin, the map order of the gag region of the feline type C viral genome has been tentatively deduced as NH2-p15-p12-p10-COOH. The demonstration of two feline leukemia virus gag gene-coded proteins, p15 and p12, expressed in the form of an uncleaved precursor in a mink cell line nonproductively transformed by feline sarcoma virus provides indirect support for the proposed sequence.
猫白血病病毒的主要非糖基化结构蛋白已被分离出来,并且针对每种蛋白都开发了竞争免疫测定法。这些蛋白包括分子量为27,000至30,000的主要内部抗原,称为p30;一种分子量为15,000的蛋白(p15);一种分子量为12,000的酸性蛋白(p12);以及一种分子量为10,000的高碱性蛋白(p10)。已鉴定出猫白血病病毒和鼠白血病病毒在免疫学和生物化学上相对应的蛋白。并且,根据与已知的源自小鼠的C型原型病毒序列的类比,猫C型病毒基因组gag区域的图谱顺序已初步推断为NH2-p15-p12-p10-COOH。在由猫肉瘤病毒非生产性转化的貂细胞系中,以未切割前体形式表达的两种猫白血病病毒gag基因编码蛋白p15和p12的证明,为所提出的序列提供了间接支持。