化学
侧链
丝氨酸
肽
氨基酸
氨基甲酸酯
组合化学
苏氨酸
异氰酸酯
酒
保护组
试剂
二肽
电泳剂
肽合成
赖氨酸
生物结合
立体化学
分子内力
环肽
有机化学
选择性
三肽
溶剂
半胱氨酸
水溶液
产量(工程)
肽键
生物分子
苯并恶唑
作者
D X Zhang,Limeng Wang,Xintao Miao,Shuai Jiang,Xiaowei Sun,Xiaoxi Xu,Jiajia Dong,Gang Lü,Xin Chu,Gong Chen
摘要
Selective labeling of alcohol side chains in peptides and proteins remains a major challenge for biomolecule modification. Herein, we report a rapid, efficient, and highly selective method for labeling both serine and threonine residues using fluorosulfuryl isocyanate (FSI) reagent in hexafluoroisopropanol (HFIP) solvent under mild conditions. The labeling reaction proceeds to completion within 1 min at room temperature, with excellent tolerance for all proteinogenic amino acid side chains except cysteine. The resulting fluorosulfuryl carbamate products can be further diversified through sulfur(VI) fluoride exchange (SuFEx) with amines to generate sulfamide-linked conjugates, or through intramolecular macrocyclization with lysine side chains to yield stapled peptides via Ser/Thr-Lys pairs. Notably, the fluorosulfuryl carbamate tag can be selectively eliminated under mildly basic aqueous conditions to generate dehydroamino acid residues, which serve as versatile electrophilic handles for one-pot conjugation with thiols, amines, or phosphines. Together, this platform offers a convenient strategy for site-selective editing of peptide alcohol side chains into structurally and functionally diverse deoxygenative analogs.
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