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Enhancers Improve the AID-Induced Hypermutation in Episomal Vector for Antibody Affinity Maturation in Mammalian Cell Display

机译:增强子可改善游离载体中AID诱导的超突变以实现哺乳动物细胞展示中的抗体亲和力成熟。

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摘要

The induction of somatic hypermutation (SHM) in various cell lines by activation-induced cytidine deaminase (AID) has been used in protein-directed selection, especially in antibody affinity maturation. Several antibody affinity maturation systems based on mammalian cells have been developed in recent years, i.e., 293T, H1299, Raji and CHO cells. However, the efficiency of in vitro AID-induced hypermutation is low, restricting the application of such systems. In this study, we examined the role of Ig and Ek enhancers in enhancing SHM in the episomal vector pCEP4 that expresses an anti-high mobility group box 1 (HMGB1) full-length antibody. The plasmid containing the two enhancers exhibited two-fold improvement of mutation rate over pCEP4 in an AID expression H1299 cell line (H1299-AID). With the engineered episomal vector, we improved the affinity of this antibody in H1299-AID cells by 20-fold.
机译:激活诱导的胞苷脱氨酶(AID)在各种细胞系中诱导体细胞超突变(SHM)已用于蛋白质定向选择,尤其是在抗体亲和力成熟中。近年来已经开发了几种基于哺乳动物细胞的抗体亲和力成熟系统,即293T,H1299,Raji和CHO细胞。然而,体外AID诱导的超突变的效率低,限制了此类系统的应用。在这项研究中,我们研究了Ig和Ek增强子在游离型载体pCEP4中增强SHM的作用,该载体表达抗高迁移性族盒1(HMGB1)全长抗体。在AID表达的H1299细胞系(H1299-AID)中,含有两种增强子的质粒比pCEP4的突变率提高了两倍。使用工程型附加型载体,我们将该抗体在H1299-AID细胞中的亲和力提高了20倍。

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