表皮生长因子受体
单克隆抗体
抗体
噬菌体展示
HEK 293细胞
生物
转染
细胞外
基因
分子生物学
体外
癌症研究
计算生物学
病毒学
遗传学
受体
作者
Eva Horak,Tara Heitner,Matthew K. Robinson,Heidi H. Simmons,Jennifer L. Garrison,Maria Russeva,Polina Furmanova,Jianlong Lou,Yu Zhou,Qing‐An Yuan,Louis M. Weiner,Gregory P. Adams,James D. Marks
标识
DOI:10.1089/cbr.2005.20.603
摘要
The members of the epidermal growth factor receptor (EGFR) family are over expressed in a variety of malignancies and are frequently linked to aggressive disease and a poor prognosis. Although clinically effective monoclonal antibodies (MAbs) have been developed to target HER2 and EGFR, the remaining two family members, HER3 and HER4, have not been the subject of significant efforts. In this paper, we have taken the initial steps required to generate antibodies with potential clinically utility that target the members of the EGFR family. The genes for the extracellular domains (ECDs) of all four members of the EGFR family were cloned and used to stably transfect 293 (HEK) cells. Milligram quantities of each ECD were produced and characterized. The HER3, HER4, and EGFR ECDs were then employed as targets for the selection of antibodies from naïve human scFv (single-chain Fv) phage display libraries. Six unique scFv clones were isolated that bound specifically to HER3, 13 unique clones were isolated with specificity for HER4 and 52 unique anti-EGFR clones were isolated. These scFvs provide a valuable and potentially clinically relevant panel of agents to target the members of the EGFR family.
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