聚糖
硫酸化
化学
硫酸可拉坦
糖基化
生物化学
糖组学
组合化学
计算生物学
糖生物学
连接器
药物发现
化学合成
表位
立体化学
模块化设计
硫酸乙酰肝素
劈开
蛋白质工程
碳水化合物构象
酶
糖胺聚糖
作者
Kaixuan Wang,Wenjing Ma,Wei Zhang,Tianhui Hao,Mengjia Zhang,Wentao Li,Wei Zhao,Zhuojia Xu,Tiehai Li
标识
DOI:10.1073/pnas.2621414123
摘要
Keratan sulfate (KS) is a unique and widely distributed glycosaminoglycans family implicated in diverse biological processes. KS features branched glycan architectures with diverse sialylation and sulfation patterns, encoding a vastly expanded chemical and biological space. The limited accessibility of well-defined structures has hindered precise investigations into the KS biological functions. Here we report a programmable chemoenzymatic platform for assembling a 106-membered library of KS N -glycans and their nonsulfated counterparts, featuring length-variable oligo- N -acetyllactosamine (LacNAc) extensions and encompassing diverse sulfation and sialylation patterns. The synthetic strategy integrates length-controlled iterative glycosylation to assemble versatile precursors, orthogonal deprotection for site-specific sulfation, and modular enzyme-driven diversification. Glycan microarray analysis of this comprehensive library reveals that glycan–protein recognition is governed by the interplay of sulfation and sialylation patterns, oligo-LacNAc chain length, and terminal epitope presentation, providing insight into the functional versatility of KS glycans.
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