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Greatest Hits—Innovative Technologies for High Throughput Identification of Bispecific Antibodies

机译:最大的匹配 - 高通量鉴定的创新技术Bispectific抗体

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摘要

Recent years have shown a tremendous increase and diversification in antibody-based therapeutics with advances in production techniques and formats. The plethora of currently investigated bi- to multi-specific antibody architectures can be harnessed to elicit a broad variety of specific modes of actions in oncology and immunology, spanning from enhanced selectivity to effector cell recruitment, all of which cannot be addressed by monospecific antibodies. Despite continuously growing efforts and methodologies, the identification of an optimal bispecific antibody as the best possible combination of two parental monospecific binders, however, remains challenging, due to tedious cloning and production, often resulting in undesired extended development times and increased expenses. Although automated high throughput screening approaches have matured for pharmaceutical small molecule development, it was only recently that protein bioconjugation technologies have been developed for the facile generation of bispecific antibodies in a ‘plug and play’ manner. In this review, we provide an overview of the most relevant methodologies for bispecific screening purposes—the DuoBody concept, paired light chain single cell production approaches, Sortase A and Transglutaminase, the SpyTag/SpyCatcher system, and inteins—and elaborate on the benefits as well as drawbacks of the different technologies.
机译:近年来,在基于抗体的治疗方法中表现出巨大的增加和多样化,具有生产技术和格式的进步。目前研究的血清素可以利用肿瘤学和免疫学中的广泛种类的特异性作用方式,从而从增强的选择性到效应细胞募集,所有这些都不能通过单特异性抗体来解决。尽管不断增长的努力和方法,因此由于繁琐的克隆和生产,鉴定了两种父母一代粘合剂的最佳组合,其两种父母单种粘合剂的最佳组合仍然是挑战性的,常常导致不希望的延长开发时间和增加的开支。虽然自动化的高通量筛选方法已经成熟用于药物小分子发育,但最近才开发了蛋白质生物杂交技术,用于在“塞子和发挥”方式中的双特异性抗体的体产生。在本文中,我们概述了双特异性筛查目的最相关的方法 - Duobody概念,配对的轻链单细胞生成方法,分类酶A和转谷氨酰胺酶,Spytag / Spycatcher系统和Inteins - 并详细说明以及不同技术的缺点。

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