Department of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, Am Muehlenberg 1, 14476, Potsdam, Germany.
Department of Chemistry and Biochemistry, Freie Universität Berlin, Arnimalle 22, 14195, Berlin, Germany.
Chemistry. 2020 Aug 6;26(44):9954-9963. doi: 10.1002/chem.202001291. Epub 2020 Jun 11.
Single glycan-protein interactions are often weak, such that glycan binding partners commonly utilize multiple, spatially defined binding sites to enhance binding avidity and specificity. Current array technologies usually neglect defined multivalent display. Laser-based array synthesis technology allows for flexible and rapid on-surface synthesis of different peptides. By combining this technique with click chemistry, neo-glycopeptides were produced directly on a functionalized glass slide in the microarray format. Density and spatial distribution of carbohydrates can be tuned, resulting in well-defined glycan structures for multivalent display. The two lectins concanavalin A and langerin were probed with different glycans on multivalent scaffolds, revealing strong spacing-, density-, and ligand-dependent binding. In addition, we could also measure the surface dissociation constant. This approach allows for a rapid generation, screening, and optimization of a multitude of multivalent scaffolds for glycan binding.
单糖-蛋白质相互作用通常较弱,因此糖结合伴侣通常利用多个空间定义的结合位点来增强结合亲和力和特异性。当前的阵列技术通常忽略了定义的多价展示。基于激光的阵列合成技术允许在表面上灵活快速地合成不同的肽。通过将该技术与点击化学相结合,可直接在功能化的玻璃载玻片上以微阵列的形式合成新型糖肽。可以调整碳水化合物的密度和空间分布,从而形成用于多价展示的定义明确的糖结构。使用不同的糖在多价支架上探测两种凝集素伴刀豆球蛋白 A 和朗格汉斯蛋白,揭示了强烈的间隔、密度和配体依赖性结合。此外,我们还可以测量表面离解常数。这种方法可以快速生成、筛选和优化多种用于糖结合的多价支架。