Evaluation of High-Affinity Monoclonal Antibodies and Antibody-Drug Conjugates by Homogenous Time-Resolved FRET

被引:0
作者
Greenway, Harmon [1 ,2 ]
Wang, Jin [1 ,2 ]
机构
[1] Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Pharmacol, Houston, TX 77030 USA
[2] Baylor Coll Med, Ctr NextGen Therapeut, Houston, TX 77030 USA
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2024年 / 15卷 / 09期
关键词
Binding Affinity; Monoclonal Antibodies; Antibody-DrugConjugates; Homogenous TR-FRET; BINDING; STABILITY;
D O I
10.1021/acsmedchemlett.4c00317
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The rapid growth of therapeutic monoclonal antibodies demands greater accessibility to scalable methods of evaluating antigen binding. Homogenous TR-FRET is ideal for preliminary screening but has not been reported to assay these interactions due to their high-affinity and complex solution-phase kinetics. Here we report the development of a competition assay to rank-order the relative affinities of these drugs for a common antigen. The assay is compatible with automation, requires no modification of the analytes, and measures affinities as low as single-digit picomolar. We further demonstrate applications to inform the development of antibody-drug conjugates. The assay may aid discovery and manufacturing of therapeutic antibodies as a low-cost, high-throughput alternative to existing technologies.
引用
收藏
页码:1598 / 1605
页数:8
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