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On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation

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 a...

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Autores principales: Mende, Marco, Tsouka, Alexandra, Heidepriem, Jasmin, Paris, Grigori, Mattes, Daniela S., Eickelmann, Stephan, Bordoni, Vittorio, Wawrzinek, Robert, Fuchsberger, Felix F., Seeberger, Peter H., Rademacher, Christoph, Delbianco, Martina, Mallagaray, Alvaro, Loeffler, Felix F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496964/
https://www.ncbi.nlm.nih.gov/pubmed/32315099
http://dx.doi.org/10.1002/chem.202001291
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author Mende, Marco
Tsouka, Alexandra
Heidepriem, Jasmin
Paris, Grigori
Mattes, Daniela S.
Eickelmann, Stephan
Bordoni, Vittorio
Wawrzinek, Robert
Fuchsberger, Felix F.
Seeberger, Peter H.
Rademacher, Christoph
Delbianco, Martina
Mallagaray, Alvaro
Loeffler, Felix F.
author_facet Mende, Marco
Tsouka, Alexandra
Heidepriem, Jasmin
Paris, Grigori
Mattes, Daniela S.
Eickelmann, Stephan
Bordoni, Vittorio
Wawrzinek, Robert
Fuchsberger, Felix F.
Seeberger, Peter H.
Rademacher, Christoph
Delbianco, Martina
Mallagaray, Alvaro
Loeffler, Felix F.
author_sort Mende, Marco
collection PubMed
description 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.
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spelling pubmed-74969642020-09-25 On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation Mende, Marco Tsouka, Alexandra Heidepriem, Jasmin Paris, Grigori Mattes, Daniela S. Eickelmann, Stephan Bordoni, Vittorio Wawrzinek, Robert Fuchsberger, Felix F. Seeberger, Peter H. Rademacher, Christoph Delbianco, Martina Mallagaray, Alvaro Loeffler, Felix F. Chemistry Full Papers 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. John Wiley and Sons Inc. 2020-06-11 2020-08-06 /pmc/articles/PMC7496964/ /pubmed/32315099 http://dx.doi.org/10.1002/chem.202001291 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Mende, Marco
Tsouka, Alexandra
Heidepriem, Jasmin
Paris, Grigori
Mattes, Daniela S.
Eickelmann, Stephan
Bordoni, Vittorio
Wawrzinek, Robert
Fuchsberger, Felix F.
Seeberger, Peter H.
Rademacher, Christoph
Delbianco, Martina
Mallagaray, Alvaro
Loeffler, Felix F.
On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation
title On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation
title_full On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation
title_fullStr On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation
title_full_unstemmed On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation
title_short On‐Chip Neo‐Glycopeptide Synthesis for Multivalent Glycan Presentation
title_sort on‐chip neo‐glycopeptide synthesis for multivalent glycan presentation
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496964/
https://www.ncbi.nlm.nih.gov/pubmed/32315099
http://dx.doi.org/10.1002/chem.202001291
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