Schultz A M, Lockhart S M, Rabin E M, Oroszlan S
J Virol. 1981 May;38(2):581-92. doi: 10.1128/JVI.38.2.581-592.1981.
The structural relationships among the gag polyproteins Pr65gag, Pr75gag, and gPr80gag of Rauscher murine leukemia virus were studied by endoglycosidase H digestion and formic acid cleavage. Fragments were identified by precipitation with specific antisera to constituent virion structural proteins followed by one-dimensional mapping. Endoglycosidase H reduced the size of gPr80gag to that of Pr75gag. By comparing fragments of gPr80gag and the apoprotein Pr75gag, the former was shown to contain two mannose-rich oligosaccharide units. By comparing fragments of Pr65gag and Pr75gag, the latter was shown to differ from Pr65gag at the amino terminus by the presence of a leader peptide approximately 7,000 daltons in size. The internal and carboxyl-terminal peptides of the two unglycosylated polyproteins were not detectably different. The location of the two N-linked carbohydrate chains in gPr80gag has been specified. One occurs in the carboxyl-terminal half of the polyprotein at asparagine177 of the p30 sequence and the other is found in a 23,000-dalton fragment located in the amino-terminal region of gPr80gag and containing the additional amino acid sequences not found in Pr65gag plus a substantial portion of p15.
通过内切糖苷酶H消化和甲酸裂解研究了劳氏鼠白血病病毒的gag多聚蛋白Pr65gag、Pr75gag和gPr80gag之间的结构关系。用针对组成病毒粒子结构蛋白的特异性抗血清沉淀,随后进行一维图谱分析来鉴定片段。内切糖苷酶H将gPr80gag的大小减小到Pr75gag的大小。通过比较gPr80gag和载脂蛋白Pr75gag的片段,发现前者含有两个富含甘露糖的寡糖单元。通过比较Pr65gag和Pr75gag的片段,发现后者在氨基末端与Pr65gag不同,存在一个大小约为7000道尔顿的前导肽。两种未糖基化多聚蛋白的内部和羧基末端肽没有明显差异。已确定gPr80gag中两条N-连接碳水化合物链的位置。一条位于多聚蛋白羧基末端的一半,在p30序列的天冬酰胺177处,另一条位于gPr80gag氨基末端区域的一个23000道尔顿的片段中,该片段包含Pr65gag中未发现的额外氨基酸序列以及大部分p15。