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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7496964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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