Bergh K, Iversen O J, Aasbakk K
Department of Microbiology, University of Trondheim, Norway.
J Immunol Methods. 1988 Apr 6;108(1-2):179-87. doi: 10.1016/0022-1759(88)90417-6.
The major zymosan-induced chemotactic factor in rabbit serum was purified by a two-step ion exchange chromatography procedure. The purified chemoattractant was used as antigen for production of murine monoclonal antibodies against the major chemotactic factor. The primary screening of the hybridoma cultures was an indirect ELISA using purified chemotactic factor as antigen. The final selection among ELISA-positive clones was performed according to the results obtained in a chemotactic inhibition assay. Six monoclonal antibodies were raised. These antibodies completely abrogated or substantially reduced the chemotactic activity in crude zymosan-activated serum. The chemotactic factor(s) could be absorbed onto an immunosorbent column containing monoclonal antibody and subsequently be specifically eluted with acid. By Western blot analysis the molecular weight of the major chemotactic factor was estimated to be approximately 15,000, and isoelectric focusing indicated a pI of about 9.4.
通过两步离子交换层析法纯化了兔血清中主要的酵母聚糖诱导趋化因子。将纯化的趋化剂用作抗原,以制备针对主要趋化因子的鼠单克隆抗体。杂交瘤培养物的初次筛选是使用纯化的趋化因子作为抗原的间接酶联免疫吸附测定(ELISA)。根据趋化抑制试验获得的结果,对ELISA阳性克隆进行最终筛选。产生了六种单克隆抗体。这些抗体完全消除或显著降低了粗制酵母聚糖激活血清中的趋化活性。趋化因子可被吸附到含有单克隆抗体的免疫吸附柱上,随后用酸特异性洗脱。通过蛋白质印迹分析,主要趋化因子的分子量估计约为15,000,等电聚焦表明其pI约为9.4。