Linciano Sara, Wong Ee Lin, Mazzocato Ylenia, Chinellato Monica, Scaravetti Tiziano, Caregnato Alberto, Cacco Veronica, Romanyuk Zhanna, Angelini Alessandro
Department of Molecular Sciences and Nanosystems, Ca' Foscari University of Venice, Mestre, Italy.
Department of Medicine (DIMED), University of Padua, Padua, Italy.
Methods Mol Biol. 2022;2491:251-262. doi: 10.1007/978-1-0716-2285-8_14.
The ability of cross-reactive antibodies to bind multiple related or unrelated targets derived from different species provides not only superior therapeutic efficacy but also a better assessment of treatment toxicity, thereby facilitating the transition from preclinical models to human clinical studies. This chapter provides some guidelines for the directed evolution of cross-reactive antibodies using yeast surface display technology. Cross-reactive antibodies are initially isolated from a naïve library by combining highly avid magnetic bead separations followed by multiple cycles of flow cytometry sorting. Once initial cross-reactive clones are identified, sequential rounds of mutagenesis and two-pressure selection strategies are applied to engineer cross-reactive antibodies with improved affinity and yet retained or superior cross-reactivity.
交叉反应抗体结合源自不同物种的多个相关或不相关靶标的能力,不仅提供了卓越的治疗效果,还能更好地评估治疗毒性,从而促进从临床前模型向人体临床研究的过渡。本章提供了一些使用酵母表面展示技术进行交叉反应抗体定向进化的指导原则。交叉反应抗体最初是通过结合高亲和力磁珠分离,然后进行多轮流式细胞术分选,从原始文库中分离出来的。一旦鉴定出初始的交叉反应克隆,就应用连续轮次的诱变和双压力选择策略来改造交叉反应抗体,以提高其亲和力,同时保留或提升交叉反应性。