Racevskis J, Sarkar N H
J Virol. 1978 Jan;25(1):374-83. doi: 10.1128/JVI.25.1.374-383.1978.
Biosynthesis of murine mammary tumor virus (MuMTV) proteins was studied in the chronically MuMTV-infected epithelial cell line MuMT-73 by using monospecific antisera to the major MuMTV core protein p27 and the major envelope glycoprotein gp47. In pulse-labeling experiments using [35S]methionine, monospecific antisera to p27 precipitated a 75,000-molecular-weight protein as the major intracellular component. Analysis of the same cellular extracts with monospecific antisera to gp47 revealed that the gp47 precursor was a 70,000-dalton protein. After chase periods, there was a loss of label from the precursors and a concomitant increase of labeled extracellular mature viral proteins. The glycoprotein precursor incorporated labeled glucosamine and seemed to be processed more rapidly than the p27 precursor. Considerable amounts of apparently nonvirion-associated gp47 and glycoprotein precursor could be detected in the extracellular culture fluid.
利用针对鼠乳腺肿瘤病毒(MuMTV)主要核心蛋白p27和主要包膜糖蛋白gp47的单特异性抗血清,在长期感染MuMTV的上皮细胞系MuMT - 73中研究了MuMTV蛋白的生物合成。在使用[35S]甲硫氨酸的脉冲标记实验中,针对p27的单特异性抗血清沉淀出一种分子量为75,000的蛋白作为主要的细胞内成分。用针对gp47的单特异性抗血清分析相同的细胞提取物表明,gp47前体是一种70,000道尔顿的蛋白。追踪一段时间后,前体中的标记物减少,同时细胞外成熟病毒蛋白的标记物增加。糖蛋白前体掺入了标记的葡糖胺,并且似乎比p27前体加工得更快。在细胞外培养液中可检测到大量明显与病毒粒子无关的gp47和糖蛋白前体。