Sugiyama K, Ishikawa R, Fukuhara N
Arch Virol. 1986;89(1-4):245-54. doi: 10.1007/BF01309893.
The structural polypeptides of the murine coronavirus DVIM (diarrhoea virus of infant mice) have been analysed in comparison with other strains MHV-2, MHV-3, MHV-4 (JHM) and MHV-S by SDS-PAGE. In the presence of 2-mercaptoethanol, three major glycopolypeptides, gp180, gp69, gp25 (as a group of similar species) and one major non-glycosylated polypeptide p58 were detected. The gp69 is a DVIM specific glycopolypeptide, in which the glycosidic moieties are linked to the core polypeptide through N-glycosidic bonds, and hence may be correlated with the short projections of the viral envelope. Further gp140, which appears in the absence of reducing agents, is apparently a dimer of gp69 held together by disulfide linkages. The gp25 family, on the other hand, consists of four polypeptides, two of which are not metabolically inhibited by tunicamycin suggesting that they are O-linked glycopolypeptides. DVIM seems to be serologically closely related to the MHV-S strain as shown by neutralization.
通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE),对鼠冠状病毒DVIM(幼鼠腹泻病毒)的结构多肽与其他毒株MHV-2、MHV-3、MHV-4(JHM)和MHV-S进行了分析比较。在2-巯基乙醇存在的情况下,检测到三种主要糖多肽gp180、gp69、gp25(作为一组相似的种类)以及一种主要的非糖基化多肽p58。gp69是DVIM特异性糖多肽,其中糖苷部分通过N-糖苷键与核心多肽相连,因此可能与病毒包膜的短突起相关。此外,在没有还原剂的情况下出现的gp140显然是由二硫键连接在一起的gp69二聚体。另一方面,gp25家族由四种多肽组成,其中两种不受衣霉素代谢抑制,表明它们是O-连接糖多肽。如中和试验所示,DVIM在血清学上似乎与MHV-S毒株密切相关。