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产生针对人成纤维细胞生长因子受体3的特异性和功能性抗体的人组合Fab文库。

Human combinatorial Fab library yielding specific and functional antibodies against the human fibroblast growth factor receptor 3.

作者信息

Rauchenberger Robert, Borges Eric, Thomassen-Wolf Elisabeth, Rom Eran, Adar Rivka, Yaniv Yael, Malka Michael, Chumakov Irina, Kotzer Sarit, Resnitzky Dalia, Knappik Achim, Reiffert Silke, Prassler Josef, Jury Karin, Waldherr Dirk, Bauer Susanne, Kretzschmar Titus, Yayon Avner, Rothe Christine

机构信息

MorphoSys AG, Lena-Christ-Strasse 48, 82152 Martinsried, Germany.

出版信息

J Biol Chem. 2003 Oct 3;278(40):38194-205. doi: 10.1074/jbc.M303164200. Epub 2003 Jul 3.

Abstract

The human combinatorial antibody library Fab 1 (HuCAL-Fab 1) was generated by transferring the heavy and light chain variable regions from the previously constructed single-chain Fv library (Knappik, A., Ge, L., Honegger, A., Pack, P., Fischer, M., Wellnhofer, G., Hoess, A., Wölle, J., Plückthun, A., and Virnekäs, B. (2000) J. Mol. Biol. 296, 57-86), diversified in both complementarity-determining regions 3 into a novel Fab display vector, yielding 2.1 x 10(10) different antibody fragments. The modularity has been retained in the Fab display and screening plasmids, ensuring rapid conversion into various antibody formats as well as antibody optimization using prebuilt maturation cassettes. HuCAL-Fab 1 was challenged against the human fibroblast growth factor receptor 3, a potential therapeutic antibody target, against which, to the best of our knowledge, no functional antibodies could be generated so far. A unique screening mode was designed utilizing recombinant functional proteins and cell lines differentially expressing fibroblast growth factor receptor isoforms diversified in expression and receptor dependence. Specific Fab fragments with subnanomolar affinities were isolated by selection without any maturation steps as determined by fluorescence flow cytometry. Some of the selected Fab fragments completely inhibit target-mediated cell proliferation, rendering them the first monoclonal antibodies against fibroblast growth factor receptors having significant function blocking activity. This study validates HuCAL-Fab 1 as a valuable source for the generation of target-specific antibodies for therapeutic applications.

摘要

人源组合抗体文库Fab 1(HuCAL-Fab 1)是通过将先前构建的单链Fv文库(Knappik, A., Ge, L., Honegger, A., Pack, P., Fischer, M., Wellnhofer, G., Hoess, A., Wölle, J., Plückthun, A., and Virnekäs, B. (2000) J. Mol. Biol. 296, 57 - 86)中的重链和轻链可变区转移到一个新型Fab展示载体中构建而成,该文库在互补决定区3中具有多样性,产生了2.1×10¹⁰种不同的抗体片段。Fab展示和筛选质粒保留了模块性,确保能够快速转化为各种抗体形式,并可使用预先构建的成熟盒进行抗体优化。针对人成纤维细胞生长因子受体3(一种潜在的治疗性抗体靶点)对HuCAL-Fab 1进行了测试,据我们所知,到目前为止尚未产生针对该靶点的功能性抗体。利用重组功能蛋白和差异表达成纤维细胞生长因子受体亚型(在表达和受体依赖性方面具有多样性)的细胞系设计了一种独特的筛选模式。通过荧光流式细胞术测定,无需任何成熟步骤,通过筛选分离出了具有亚纳摩尔亲和力的特异性Fab片段。一些选定的Fab片段完全抑制靶点介导的细胞增殖,使其成为首批具有显著功能阻断活性的抗成纤维细胞生长因子受体单克隆抗体。本研究验证了HuCAL-Fab 1作为用于治疗应用的靶点特异性抗体产生的宝贵来源。

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