Kruppa J
Biochem J. 1979 Aug 1;181(2):295-300. doi: 10.1042/bj1810295.
I studied the glycosylation in vivo of a viral envelope protein, the glycoprotein of vesicular stomatitis virus (VSV), by pulse labelling of virus-infected HeLa cells with 3H-labelled monosaccharides (mannose, glucosamine). Radioactivity was incorporated into the fraction of membrane-bound polyribosomes, although metabolic conversion of [3H]-mannose into amino acids was negligible. Dissociation of bound polyribosomes revealed that the radioactively co-purified with the peptidyl-tRNA. The nascent peptides were released by alkaline hydrolysis, immunoprecipitated and analysed by polyacrylamide-gel electrophoresis. It is apparent from the size distribution of the [3H]mannose-labelled nascent chains that attachment of carbohydrate starts when approximately half of the amino acid sequence of the viral glycoprotein has been synthesized.
我通过用³H标记的单糖(甘露糖、葡糖胺)对感染病毒的HeLa细胞进行脉冲标记,研究了病毒包膜蛋白(水疱性口炎病毒糖蛋白)在体内的糖基化情况。放射性被掺入膜结合多核糖体部分,尽管[³H]甘露糖向氨基酸的代谢转化可忽略不计。结合的多核糖体解离显示,放射性与肽基tRNA共纯化。新生肽通过碱性水解释放,进行免疫沉淀并通过聚丙烯酰胺凝胶电泳分析。从[³H]甘露糖标记的新生链的大小分布可以明显看出,当病毒糖蛋白的氨基酸序列大约合成一半时,碳水化合物开始附着。