Conlon P J, Luk K H, Park L S, March C J, Hopp T P, Urdal D L
J Immunol. 1985 Jul;135(1):328-32.
The colony-stimulating factor CSF-2 alpha (IL 3) has been purified to homogeneity, the protein sequenced, and the gene encoding this lymphokine cloned. Knowledge of the protein sequence permitted the synthesis of peptides corresponding to the amino terminus of the molecule. These peptides, after conjugation to palmitic acid, were used to immunize mice. Spleen cells from mice immunized with one of these peptides (CSF-2 alpha 1-14) were fused with the myeloma cell line NS-1. The fusion resulted in the isolation of two hybridoma cell lines, designated 6A5 and 4D4, that secreted antibodies that were specific for the immunizing peptide. The antibodies did not react with a closely related peptide CSF-2 alpha 7-16. The antibodies were capable, however, of recognized CSF-2 alpha protein as judged by the ability of the antibodies to remove CSF-2 alpha activity from culture medium of PHA-stimulated LBRM-33-5A4 cells, to immunoprecipitate radiolabeled CSF-2 alpha protein, and to detect CSF-2 alpha protein bound to nitrocellulose membranes.
集落刺激因子CSF - 2α(白细胞介素3)已被纯化至同质,测定了该蛋白质的序列,并克隆了编码此淋巴因子的基因。蛋白质序列的信息使得能够合成与该分子氨基末端相对应的肽段。这些肽段与棕榈酸偶联后,用于免疫小鼠。用其中一种肽段(CSF - 2α1 - 14)免疫的小鼠脾细胞与骨髓瘤细胞系NS - 1融合。融合后分离出两个杂交瘤细胞系,命名为6A5和4D4,它们分泌对免疫肽具有特异性的抗体。这些抗体不与密切相关的肽段CSF - 2α7 - 16发生反应。然而,通过抗体从PHA刺激的LBRM - 33 - 5A4细胞培养基中去除CSF - 2α活性、免疫沉淀放射性标记的CSF - 2α蛋白以及检测与硝酸纤维素膜结合的CSF - 2α蛋白的能力判断,这些抗体能够识别CSF - 2α蛋白。