结合
连接器
化学
组合化学
抗体
环加成
Diels-Alder反应
抗体-药物偶联物
立体化学
单克隆抗体
生物化学
生物
免疫学
催化作用
数学分析
数学
计算机科学
操作系统
作者
Thomas Nittoli,Sylvia J. Degrado,Hamid Samareh Afsari,Puneet Anand,Jeffrey Bos,Seung-Yong Choi,Emily Mallett,Tom Markotan,Jan Spink,Marvin Vega,Mrinmoy Saha,Robert L. Schuster,Ji Jiang,Jieyu Zhou,Anna Brotcke Zumsteg,Alida Coppi,Susan Jorgenson,Stephanie Federici,Haiting Zhang,Jasmine Moustakas,Christopher D’Souza,Christos A. Kyratsous,William C. Olson
标识
DOI:10.1016/j.xcrp.2023.101544
摘要
Antibody-drug conjugates (ADCs) have emerged as a formidable class of targeted biologics. Whereas all 11 Food and Drug Administration-approved ADCs are based on random conjugation, accumulating evidence suggests a potential for improved therapeutic index with site-specific ADCs. Here, we present a two-step sequential conjugation approach that marries the site specificity of the bacterial transglutaminase (TG) reaction with the robustness of Diels-Alder (DA) chemistry to generate stable antibody conjugates with favorable physiochemical properties. Further, we identify diene-based linkers with different reaction kinetics for DA coupling, and we use these linker derivatives to conjugate antibodies to two distinct small molecules in tandem. In addition, we show strong potency of antibody conjugates, prepared via TG-DA chemistry, in both cell-based assays and a mouse model. Overall our conjugation approach is site specific, versatile, and can potentially be used to generate different classes of antibody conjugates for multiple therapeutic areas.
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