Laboratory of Organic Chemistry, Wageningen University & Research, Stippeneng 4, 6708 WE, Wageningen, The Netherlands.
Synaffix BV, Kloosterstraat 9, 5349 AB, Oss, The Netherlands.
Bioconjug Chem. 2021 Oct 20;32(10):2167-2172. doi: 10.1021/acs.bioconjchem.1c00351. Epub 2021 Sep 14.
The availability of tools to generate homogeneous and stable antibody conjugates without recombinant DNA technology is a valuable asset in fields spanning from diagnostics to imaging and therapeutics. We present here a general approach for the conjugation to human IgG1 antibodies, by employing a straightforward two-stage protocol based on antibody deglycosylation followed by tyrosinase-mediated -quinone strain-promoted click chemistry. The technology is validated by the efficient and clean generation of highly potent DAR2 and DAR4 antibody-drug conjugates (ADCs) with cytotoxic payloads MMAE or PBD dimer, and their evaluation.
在从诊断到成像和治疗等多个领域,拥有无需重组 DNA 技术即可生成均质且稳定的抗体偶联物的工具是一项宝贵的资产。我们在此提出了一种通用方法,可通过基于抗体去糖基化,然后进行漆酶介导的 - 醌应变促进点击化学的两步法方案,将其偶联至人 IgG1 抗体上。该技术通过高效且清洁地生成具有细胞毒性有效载荷 MMAE 或 PBD 二聚体的高 DAR2 和 DAR4 抗体药物偶联物 (ADC) 得到验证,并对其进行了评估。