Keck Zhen-Yong, Wang Yong, Lau Patrick, Foung Steven K H
Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Methods Mol Biol. 2019;1911:395-419. doi: 10.1007/978-1-4939-8976-8_27.
Yeast surface display (YSD) enables efficient screening and selection of single chain variable fragments (scFvs) of heavy (V) and light (V) chains that bind to target antigen with different affinities. Assembly of a scFv library from cDNA usually involves adding different primers and linkers (Gly/Ser) through multiple rounds of PCR amplification and purification. We describe here a simplified scFv assembly method by creating a modified YSD vector with a built-in linker that reduces the time of assembly and decreases accumulated base exchanges due to PCR errors. In addition, we describe a bias screening strategy toward maximizing novel antibodies of interest by a combination of memory B cell selection and depletion by binding to mutant antigens that do not bind to previously identified monoclonal antibodies.
酵母表面展示(YSD)能够高效筛选和选择具有不同亲和力与靶抗原结合的重链(V)和轻链(V)单链可变片段(scFv)。从cDNA组装scFv文库通常需要通过多轮PCR扩增和纯化添加不同的引物和接头(甘氨酸/丝氨酸)。我们在此描述一种简化的scFv组装方法,通过创建一种带有内置接头的改良YSD载体,减少组装时间并减少由于PCR错误导致的累积碱基交换。此外,我们描述了一种偏向性筛选策略,通过结合记忆B细胞选择和与先前鉴定的单克隆抗体不结合的突变抗原结合来耗尽,从而最大化感兴趣的新型抗体。