多特异性抗体格式的工程技术和生物分析

M. Amaral, Soraya Hölper, Christian Lange, Jennifer Jung, H. Sjuts, Sandra Weil, M. Fischer, Katarina Radoevic, Ercole Rao
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引用次数: 5

摘要

设计能够同时结合相同或不同抗原上的两个或多个表位的多特异性抗体的想法是在50多年前发展起来的。然而,这些分子的分子复杂性可能对其开发和临床应用构成重大挑战。尤其具有挑战性的是获得不同多肽链的正确组装组合,这对下游工艺开发、分析表征和控制策略提出了重大要求。在这里,我们回顾了蛋白质工程的进展,以迫使不同的重链和轻链的正确组装,以及上游和下游工艺目前用于控制产生不需要的副产物。我们深入介绍了可用于表征这种复杂分子的分析方法,重点是错配分析和功能表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineered Technologies and Bioanalysis of multispecific Antibody Formats
The idea of designing multispecific antibodies capable of simultaneously engaging two or more epitopes on the same or different antigens was developed more than 50 years ago. However, the molecular complexity of such molecules may pose significant challenges for their development and clinical use. Particularly challenging is to obtain the correctly assembled combination of different polypeptide chains, which places significant demand on downstream process development, analytical characterization and control strategy. Here, we review the progress made in protein engineering to force the correct assembly of different heavy and light chains, as well as upstream and downstream processes currently applied to control generation of unwanted byproduct species. We cover in-depth the analytical methods available to characterize such complex molecules, focusing on mispairing analysis and functional characterization.
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