Blair Zajdel M E, Barker M D, Dixon S C, Blair G E
Biochem J. 1985 Feb 1;225(3):649-55. doi: 10.1042/bj2250649.
Monoclonal antibodies against two of the proteins specified by one of the transforming genes (early region 1B) of human adenovirus type 2 have been produced and characterized. Two clones (RA1 and PA6), generated by fusion of mouse myeloma NSO cells with splenocytes from rats immunized with whole-cell lysates of an adenovirus-transformed rat cell line (F19), secreted antibodies against a 58 kDa protein. Another clone (DC1) produced antibodies against the same protein, and resulted from fusion of immune rat splenocytes with the rat myeloma Y3.Ag.1.2.3. Immunoprecipitation studies showed that all three antibodies recognized [35S]-methionine-labelled 58 kDa protein, and phosphorylated derivatives of the 58 kDa protein labelled with [32P]orthophosphate present in infected human cells. One clone (EC3) produced antibody against a 19 kDa protein also encoded by early region 1B, but not sharing sequence homology with 58 kDa. The identity of the 19 kDa protein recognized by the EC3 antibody was established by immunoprecipitation from lysates of labelled-infected cells and from products of cell-free translation directed by mRNA isolated from adenovirus 2-infected cells. Indirect immunofluorescent-antibody staining of infected human cells using the RA1 and EC3 antibodies revealed a nuclear location of the 58 kDa protein and a mainly cytoplasmic location of the 19 kDa protein.
已制备并鉴定出针对人腺病毒2型一种转化基因(早期区域1B)所指定的两种蛋白质的单克隆抗体。通过将小鼠骨髓瘤NSO细胞与用腺病毒转化的大鼠细胞系(F19)的全细胞裂解物免疫的大鼠脾细胞融合产生的两个克隆(RA1和PA6),分泌针对一种58 kDa蛋白质的抗体。另一个克隆(DC1)产生针对相同蛋白质的抗体,它是由免疫大鼠脾细胞与大鼠骨髓瘤Y3.Ag.1.2.3融合产生的。免疫沉淀研究表明,所有三种抗体都识别[35S] - 甲硫氨酸标记的58 kDa蛋白质,以及感染的人细胞中存在的用[32P]正磷酸盐标记的58 kDa蛋白质的磷酸化衍生物。一个克隆(EC3)产生针对一种也由早期区域1B编码但与58 kDa不具有序列同源性的19 kDa蛋白质的抗体。通过从标记感染细胞的裂解物以及从腺病毒2感染细胞分离的mRNA指导的无细胞翻译产物中进行免疫沉淀,确定了EC3抗体识别的19 kDa蛋白质的身份。使用RA1和EC3抗体对感染的人细胞进行间接免疫荧光抗体染色,结果显示58 kDa蛋白质位于细胞核,而19 kDa蛋白质主要位于细胞质。