Mardassi H, Gonin P, Gagnon C A, Massie B, Dea S
Centre de Recherche en Virologie, Institut Armand-Frappier, Université du Québec, Laval, Québec, Canada H7N 4Z3.
J Virol. 1998 Aug;72(8):6298-306. doi: 10.1128/JVI.72.8.6298-6306.1998.
The GP3 protein of the IAF-Klop strain of porcine reproductive and respiratory syndrome virus (PRRSV) was expressed in 293 cells by a recombinant human type 5 adenovirus carrying the open reading frame 3 gene. The protein exhibited a molecular mass of 42 kDa and comigrated with GP3 expressed in PRRSV-infected MARC-145 cells. Removal of N-linked glycans from GP3 resulted in a 27-kDa protein (P3), confirming its highly glycosylated nature. Pulse-chase experiments carried out either in the context of PRRSV infection or upon individual expression of GP3 in 293 cells showed that the protein remains completely endo-beta-N-acetylglucosaminidase H-sensitive even after 4 h of synthesis. Thus, the transport of GP3 was restricted to the premedial Golgi compartment, presumably the endoplasmic reticulum (ER). However, a minor fraction of GP3 was found to be secreted in the culture medium as a soluble membrane-free form. This released protein (sGP3) was readily identified upon individual expression of GP3 in 293 cells as well as in the context of PRRSV infection, albeit at lower levels. The sGP3 migrated as a smear and displayed a molecular mass ranging from 43 to 53 kDa. The unglycosylated form of sGP3 comigrated with its intracellular deglycosylated counterpart, suggesting that the release from the cell of a subset of GP3 did not result from cleavage of a putative membrane-anchor sequence. Strikingly, unlike GP3, the sGP3 acquired Golgi-specific modifications of its carbohydrate side chains and folded into a disulfide-linked homodimer. Brefeldin A treatment completely abolished the release of sGP3, suggesting that the ER-to-Golgi compartment is an obligatory step in cellular secretion of sGP3. In contrast, 10 mM monensin did not prevent sGP3 release but inhibited the terminal glycosylation that confers on the protein its diffuse pattern. Since GP3 was found to be nonstructural in the case of the North American strain, secretion of a minor fraction of GP3 might be an explanation for its high degree of immunogenicity in infected pigs. Furthermore, this secreted protein might be relevant as a model for further studies on the cellular subcompartments involved in the sorting of proteins to the extracellular milieu.
通过携带开放阅读框3基因的重组人5型腺病毒,在293细胞中表达了猪繁殖与呼吸综合征病毒(PRRSV)IAF-Klop株的GP3蛋白。该蛋白分子量为42 kDa,与PRRSV感染的MARC-145细胞中表达的GP3迁移率相同。去除GP3上的N-连接聚糖后得到一个27 kDa的蛋白(P3),证实了其高度糖基化的性质。在PRRSV感染的情况下或在293细胞中单独表达GP3后进行的脉冲追踪实验表明,即使在合成4小时后,该蛋白仍完全对内切β-N-乙酰葡糖胺酶H敏感。因此,GP3的转运局限于高尔基体前区室,可能是内质网(ER)。然而,发现一小部分GP3以可溶性无膜形式分泌到培养基中。在293细胞中单独表达GP3以及在PRRSV感染的情况下,都很容易鉴定出这种释放的蛋白(sGP3),尽管其水平较低。sGP3迁移时呈拖尾状,分子量范围为43至53 kDa。sGP3的未糖基化形式与其细胞内去糖基化的对应物迁移率相同,这表明GP3的一部分从细胞中释放并非来自假定的膜锚定序列的切割。引人注目的是,与GP3不同,sGP3获得了其碳水化合物侧链的高尔基体特异性修饰,并折叠成二硫键连接的同型二聚体。布雷菲德菌素A处理完全消除了sGP3的释放,这表明内质网到高尔基体区室是sGP3细胞分泌过程中的一个必要步骤。相比之下,10 mM莫能菌素并不能阻止sGP3的释放,但会抑制赋予该蛋白其弥散模式的末端糖基化。由于在北美毒株中发现GP3是非结构性的,一小部分GP3的分泌可能解释了其在感染猪中的高免疫原性。此外,这种分泌蛋白可能作为进一步研究参与蛋白质分选到细胞外环境的细胞亚区室的模型具有相关性。