Department of Chemistry and Interdisciplinary Nanoscience Centre (iNANO), Aarhus University, Gustav Wieds Vej 14, 8000, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Brendstrupgårdsvej 21A, 8200, Aarhus N, Denmark.
Angew Chem Int Ed Engl. 2021 Mar 15;60(12):6539-6544. doi: 10.1002/anie.202013911. Epub 2021 Feb 3.
Functionalized antibodies are an indispensable resource for diagnosis, therapy and as a research tool for chemical biology. However, simpler and better methodologies are often required to improve the labeling of antibodies in terms of selectivity and scalability. Herein, we report the development of an easily available chemical reagent that allows site-directed labeling of native human IgG1 antibodies in good yield and mono-labeling selectivity. The salicylaldehyde moiety of the reagent reacts with surface exposed lysine residues to transiently form an iminium ion, and this positions a semi-reactive ester in proximity of a second lysine residue that reacts with the ester to form an amide. Interestingly, it appears that the formation of the iminium ion also has a significant activating effect of the ester. We use flow cytometry and bio-layer interferometry to confirm that the labeled antibodies retain antigen binding.
功能化抗体是诊断、治疗以及作为化学生物学研究工具不可或缺的资源。然而,通常需要更简单、更好的方法来提高抗体的标记选择性和可扩展性。在此,我们报告了一种易于获得的化学试剂的开发,该试剂可高产率和单标记选择性地实现天然人 IgG1 抗体的定点标记。该试剂的水杨醛部分与表面暴露的赖氨酸残基反应,瞬时形成亚胺离子,这使半反应性酯靠近第二个赖氨酸残基,该赖氨酸残基与酯反应形成酰胺。有趣的是,形成亚胺离子似乎对酯也有显著的激活作用。我们使用流式细胞术和生物层干涉技术来确认标记的抗体保留抗原结合。