重组DNA
单克隆抗体
免疫球蛋白Fab片段
抗体
亲和层析
化学
转染
施耐德2号电池
大小排阻色谱法
分子生物学
细胞培养
生物化学
抗原
生物
酶
基因
遗传学
互补决定区
RNA干扰
核糖核酸
作者
Marija Backović,Daniel X. Johansson,Barbara G. Klupp,Thomas C. Mettenleiter,Mats A. A. Persson,F.A. Rey
标识
DOI:10.1093/protein/gzp088
摘要
Fab molecules are used as therapeutic agents, and are invaluable tools in structural biology. We report here a method for production of recombinant Fab in Drosophila S2 cells for use in structural biology. Stably transfected S2 cell lines expressing the Fab were created within weeks. The recombinant Fab was secreted, and after affinity and size exclusion chromatography, 16 mg of pure protein were obtained from a liter of cell culture. The Fab was functional and formed a complex with its cognate antigen as demonstrated by co-precipitation and size exclusion chromatography. Biochemical characterization indicated that the Fab from S2 cells is less extensively glycosylated than the Fab obtained by digestion of antibody produced in hybridoma cells, a feature that may be advantageous for the purposes of crystallogenesis. Taken together, obtaining recombinant Fab from the S2 cells has been a faster and considerably more cost-effective method compared with the enzymatic digestion of the monoclonal antibody.
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