化学选择性
化学结扎
肽
酶
化学
表面改性
组合化学
肽生物合成
氨基酸
区域选择性
肽合成
生物催化
羧酸
水溶液
生物结合
肽序列
酶催化
有机化学
化学合成
结扎
作者
Jay Hanssens,Sam van Dun,Tessa H.G. Lokate,Vincent R.A.M. Reinartz,Leendert J. van den Bos,Romano V. A. Orrù,Jordy M. Saya
标识
DOI:10.1016/j.xcrp.2025.102860
摘要
Peptide and protein synthesis, as well as bioconjugation, are increasingly important for developing site-selective modifications in biomedical applications. Herein, we report a strategy that combines the Passerini multicomponent reaction and peptiligase-mediated ligations for the selective bio-conjugation of peptide C-termini. The Passerini reaction, performed under aqueous acidic buffer conditions, ensures chemoselectivity for the carboxylic acids, while the subsequent enzymatic ligation selectively targets the functionalized C-terminal substrates. We demonstrated this approach on a diverse set of peptides while incorporating various isocyanides and aldehydes/ketones and successfully achieved ligations. By combining the Passerini reaction with enzymatic selectivity, this method provides a versatile and efficient platform for site-selective C-terminal modification, expanding the toolkit for peptide and protein modifications and synthesis. • Functionalization and subsequent ligation of unprotected peptides • Chemoselective Passerini functionalization of carboxylic acids on peptides • Use of aqueous buffer conditions in all steps • Regio- and diastereoselective enzymatic ligation at the C-terminus Hanssens et al. present a selective bio-conjugation strategy for peptide C-termini, combining the Passerini multicomponent reaction and chemo-enzymatic peptide synthesis (CEPS). Aqueous acidic buffer conditions ensure chemoselectivity for carboxylic acids, followed by regioselective enzymatic ligation at the C-termini. This approach opens new avenues for site-selective peptide and protein modifications.
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