Espinoza A M, Usmany M, Pirone T P, Harvey M, Woolston C J, Medina V, Vlak J M, Hull R
Cellular and Molecular Biology Research Center (CIBCM), University of Costa Rica, San José.
Intervirology. 1992;34(1):1-12. doi: 10.1159/000150257.
The cauliflower mosaic virus ORF II encoding the aphid transmission factor (ATF) was mutagenized to introduce a BamHI restriction site upstream from the initiation codon and then cloned into an eukaryotic viral expression vector (Autographa californica nuclear polyhedrosis virus). All recombinant viruses tested in Spodoptera frugiperda (SF21) cells expressed a protein of about 18 kD which comigrated in PAGE with ATF from infected plants. Western blotting using an oligopeptide antiserum to ATF confirmed the identity of the 18-kD protein from infected cells as the product of the ORF II sequences (P18). Subcellular fractionation of cells infected with the recombinant AcMNPV demonstrated that the expressed P18 accumulated intracellularly in an insoluble form. Antiserum was produced in rabbit against the partially purified P18 expressed in SF21 cells. When used to immunogold label ultrathin sections of cauliflower mosaic virus (CaMV)-infected turnip tissue, this antiserum was shown to be highly specific, labelling only the electronlucent inclusion bodies (containing P18) and not other plant cellular components.
对编码蚜虫传播因子(ATF)的花椰菜花叶病毒开放阅读框II进行诱变,以在起始密码子上游引入一个BamHI限制性酶切位点,然后将其克隆到真核病毒表达载体(苜蓿银纹夜蛾核多角体病毒)中。在草地贪夜蛾(SF21)细胞中测试的所有重组病毒都表达了一种约18 kD的蛋白质,该蛋白质在聚丙烯酰胺凝胶电泳(PAGE)中与来自受感染植物的ATF迁移率相同。使用针对ATF的寡肽抗血清进行的蛋白质免疫印迹法证实,来自受感染细胞的18-kD蛋白质是开放阅读框II序列(P18)的产物。对感染重组苜蓿银纹夜蛾核多角体病毒(AcMNPV)的细胞进行亚细胞分级分离表明,表达的P18以不溶性形式在细胞内积累。用兔针对在SF21细胞中表达的部分纯化的P18制备抗血清。当用于对花椰菜花叶病毒(CaMV)感染的芜菁组织超薄切片进行免疫金标记时,该抗血清显示出高度特异性,仅标记电子透明包涵体(含有P18),而不标记其他植物细胞成分。