Adler C J, Elzinga M, Wimmer E
J Gen Virol. 1983 Feb;64 (Pt 2):349-55. doi: 10.1099/0022-1317-64-2-349.
VPg, the genome-linked protein of poliovirus, and its putative precursor P3-9, were radiolabelled and subjected to carboxypeptidase-A digestion. The release of amino acids was followed by identification and quantification on an amino acid analyser. Both proteins were found to be co-terminal with a sequence of -valyl-glutamine-COOH, an observation that provides further evidence that host cell trimming of virus-specific peptides does not play a role in poliovirus protein processing. Radiolabelled VPg was subjected to automated Edman degradation. The combined results complete the structural analysis of VPg, a polypeptide 22 amino acids in length with a molecular weight of 2354. Only one form of VPg has been found linked to virion RNA and it originates by a cleavage at glutaminyl-glycine pairs at both termini. The observation is consistent with other cleavages found in the virus processing scheme.
脊髓灰质炎病毒的基因组连接蛋白VPg及其假定的前体P3-9被放射性标记,并进行羧肽酶A消化。氨基酸释放后,在氨基酸分析仪上进行鉴定和定量。发现这两种蛋白质的C末端均为-缬氨酰-谷氨酰胺-COOH序列,这一观察结果进一步证明宿主细胞对病毒特异性肽的修剪在脊髓灰质炎病毒蛋白加工过程中不起作用。对放射性标记的VPg进行自动Edman降解。综合结果完成了对VPg的结构分析,VPg是一种由22个氨基酸组成、分子量为2354的多肽。仅发现一种形式的VPg与病毒粒子RNA相连,它是通过两端谷氨酰胺-甘氨酸对处的切割产生的。这一观察结果与病毒加工过程中发现的其他切割情况一致。