TY - JOUR
T1 - On-Chip Neo-Glycopeptide Synthesis for Multivalent Glycan Presentation
AU - Mende, Marco
AU - Tsouka, Alexandra
AU - Heidepriem, Jasmin
AU - Paris, Grigori
AU - Mattes, Daniela S.
AU - Eickelmann, Stephan
AU - Bordoni, Vittorio
AU - Wawrzinek, Robert
AU - Fuchsberger, Felix F.
AU - Seeberger, Peter H.
AU - Rademacher, Christoph
AU - Delbianco, Martina
AU - Mallagaray, Alvaro
AU - Loeffler, Felix F.
N1 - Funding Information:
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.
Publisher Copyright:
© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/8/6
Y1 - 2020/8/6
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85086320376&partnerID=8YFLogxK
U2 - 10.1002/chem.202001291
DO - 10.1002/chem.202001291
M3 - Journal articles
C2 - 32315099
AN - SCOPUS:85086320376
SN - 0947-6539
VL - 26
SP - 9954
EP - 9963
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 44
ER -