Site-Specific Dual Antibody Conjugation via Engineered Cysteine and Selenocysteine Residues

通过工程改造的半胱氨酸和硒代半胱氨酸残基实现位点特异性双抗体结合

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作者:Xiuling Li, James T Patterson, Mohosin Sarkar, Lee Pedzisa, Thomas Kodadek, William R Roush, Christoph Rader

Abstract

Site-specific conjugation technologies enable the production of homogeneous antibody-drug conjugates (ADCs) with improved therapeutic indices compared to conventional ADCs. However, current site-specific conjugation methods can only attach one type of drug to a single antibody. Given the emergence of acquired resistance to current ADCs, arming single antibodies with different drugs may provide an attractive option in the development of next-generation ADCs. Here, we describe a site-specific dual conjugation strategy as a platform for dual warhead ADCs.

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