Ilyinskii P O, Morozov V A, Ilyin K V
All-Union Cancer Research Center, Moscow, U.S.S.R.
Arch Virol. 1990;110(3-4):295-9. doi: 10.1007/BF01311298.
The study of the gag-coded glycosylated polyprotein (gPr78gag) from type D retrovirus-producing cells is reported. It is shown that glycosylation inhibitors tunicamycin and 2-deoxy-D-glucose are blocking the synthesis of gPr78gag. This demonstrates that gPr78gag is a N-glycan. The protein part of gPr78gag is supposedly identified (MW = 65 k). The inhibitors used partially stopped the processing of gag-coded polyprotein Pr78gag into core protein p27 as shown in pulse-chase experiments.
本文报道了对来自产生D型逆转录病毒的细胞中的gag编码糖基化多蛋白(gPr78gag)的研究。结果表明,糖基化抑制剂衣霉素和2-脱氧-D-葡萄糖可阻断gPr78gag的合成。这表明gPr78gag是一种N-聚糖。推测已鉴定出gPr78gag的蛋白质部分(分子量 = 65k)。如脉冲追踪实验所示,所使用的抑制剂部分阻止了gag编码的多蛋白Pr78gag加工成核心蛋白p27。