Abstract
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.
| Original language | English |
|---|---|
| Journal | Chemistry - A European Journal |
| Volume | 26 |
| Issue number | 44 |
| Pages (from-to) | 9954-9963 |
| Number of pages | 10 |
| ISSN | 0947-6539 |
| DOIs | |
| Publication status | Published - 06.08.2020 |
Funding
This research was supported by the German Federal Ministry of Education and Research [BMBF, grant number 13XP5050A], the MPG‐FhG cooperation [Glyco3Display], and the Max Planck Society.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Research Areas and Centers
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)
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