Takahashi-Omoe H, Omoe K, Matsushita S, Inada T
Department of Technical Support and Development, National Institute of Radiological Science, 4-9-1 Anagawa, Inage-Ku, Chiba-shi 263-8555, Japan.
Comp Immunol Microbiol Infect Dis. 2004 Nov;27(6):423-31. doi: 10.1016/j.cimid.2004.01.003.
Lactate dehydrogenase-elevating virus (LDV) has a strict species-specificity and can replicate only in a subset of mouse primary macrophages in vitro. Because it is difficult to grow and purify sufficient quantities of LDV virions from the primary macrophages, it has been difficult to further characterize LDV envelope proteins. A few expression systems have been reported for structural analysis of the nonglycosylated envelope protein M/VP-2, however, very few studies of the antigenicity of M/VP-2 have been reported. We cloned and expressed the ORF6 gene, which encodes the M/VP-2, as a fusion protein with a polyhistidine metal-binding tag (6 x His-tag) in Autographa californica nuclear polyhedrosis virus (baculovirus) under the control of the polyhedrin promoter. In Western blotting analysis, the expressed protein was similar in size to the native M/VP-2 plus 6 x His-tag. The usefulness of the baculovirus-expressed LDV ORF6 protein for analysis of the immunogenicity of LDV M/VP-2 was discussed.
乳酸脱氢酶升高病毒(LDV)具有严格的种属特异性,在体外仅能在一部分小鼠原代巨噬细胞中复制。由于从原代巨噬细胞中培养和纯化足够数量的LDV病毒粒子很困难,因此进一步表征LDV包膜蛋白一直存在困难。已经报道了一些用于非糖基化包膜蛋白M/VP-2结构分析的表达系统,然而,关于M/VP-2抗原性的研究报道却很少。我们克隆并表达了编码M/VP-2的ORF6基因,在多角体蛋白启动子的控制下,将其作为与多组氨酸金属结合标签(6×His标签)融合的蛋白,在苜蓿银纹夜蛾核型多角体病毒(杆状病毒)中表达。在蛋白质印迹分析中,表达的蛋白大小与天然M/VP-2加上6×His标签相似。讨论了杆状病毒表达的LDV ORF6蛋白在分析LDV M/VP-2免疫原性方面的用途。