Center for Nanomedicine and Theranostics, Department of Chemistry, Technical University of Denmark , Kemitorvet, Building 207, 2800 Kgs. Lyngby, Denmark.
Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces , Am Mühlenberg 1, 14476 Potsdam, Germany.
J Org Chem. 2017 Dec 1;82(23):12066-12084. doi: 10.1021/acs.joc.7b01796. Epub 2017 Nov 20.
The synthesis of linear and (1 → 6)-branched β-(1 → 3)-d-galactans, structures found in plant arabinogalactan proteins (AGPs), is described. The synthetic strategy relies on iterative couplings of monosaccharide and disaccharide thioglycoside donors, followed by a late-stage glycosylation of heptagalactan backbone acceptors to introduce branching. A key finding from the synthetic study was the need to match protective groups in order to tune reactivity and ensure selectivity during the assembly. Carbohydrate microarrays were generated to enable the detailed epitope mapping of two monoclonal antibodies known to recognize AGPs: JIM16 and JIM133.
线性和(1 → 6)-支链β-(1 → 3)-半乳糖苷的合成,这些结构存在于植物阿拉伯半乳聚糖蛋白(AGPs)中,被描述。合成策略依赖于单糖和二糖硫糖苷供体的迭代偶联,然后对七半乳糖苷主链受体进行晚期糖基化以引入支链。合成研究的一个关键发现是需要匹配保护基团,以在组装过程中调节反应性并确保选择性。生成了碳水化合物微阵列,以能够对两种已知识别 AGP 的单克隆抗体 JIM16 和 JIM133 进行详细的表位作图。