体细胞突变
亲和力成熟
抗体
化学
细胞生物学
抗原
生物物理学
特异性抗体
蛋白质工程
脚手架
计算生物学
体细胞
生物
免疫球蛋白Fab片段
突变
嫁接
血浆蛋白结合
蛋白质稳定性
作者
Audrey D. McConnell,V. Spasojevich,John L. Macomber,Irina Krapf,Athena Chen,Joseph C Sheffer,Ashley D. Berkebile,Robert A. Horlick,S Neben,David J. King,Peter M. Bowers
标识
DOI:10.1093/protein/gzs090
摘要
Antibodies are important tools for a broad range of applications due to their high specificity and ability to recognize virtually any target molecule. However, in order to be practically useful, antibodies must be highly stable and bind their target antigens with high affinity. We present a combinatorial approach to generate high-affinity, highly stable antibodies through the design of stable frameworks, specificity grafting and maturation via somatic hypermutation in vitro. By collectively employing these methods, we have engineered a highly stable, high-affinity, full-length antibody with a T(m) over 90°C that retains significant activity after heating to 90°C for 1 h, and has ~95-fold improved antigen-binding affinity. The stabilized IgG framework is compatible with affinity maturation, and should provide a broadly useful scaffold for grafting a variety of complementarity-determining region loops for the development of stable antibodies with desired specificities.
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