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Novel approaches to design glycan-based antibacterial inhibitors
Umeå University, Faculty of Science and Technology, Department of Chemistry.ORCID iD: 0000-0002-9835-7045
Umeå University, Faculty of Science and Technology, Department of Chemistry.ORCID iD: 0000-0002-4841-6238
2023 (English)In: European Journal of Organic Chemistry, ISSN 1434-193X, E-ISSN 1099-0690, Vol. 26, no 1, article id e202200795Article, review/survey (Refereed) Published
Abstract [en]

The interactions between bacterial lectins and carbohydrates on the host cell surface can mediate bacterial adhesion, invasion, and immune evasion. Multivalency plays a key role in these binding events. However, additional molecular mechanisms greatly impact multivalent binding recognition. To develop specific and effective bacterial inhibitors, a deeper understanding of the complex underlying mechanisms of bacterial adhesion processes is necessary. By interfering with bacterial adhesion, synthetic multivalent glycoconjugates do not only have the potential to improve or replace antibiotic treatments, but also represent useful tools to study carbohydrate-pathogen interactions. In this review, we highlight a few recent advances in the synthesis and application of synthetic glycan-based scaffolds to uncover the nature of glycan-bacteria interactions and to design efficient bacterial inhibitors.

Place, publisher, year, edition, pages
John Wiley & Sons, 2023. Vol. 26, no 1, article id e202200795
Keywords [en]
Bacteria, Glycoconjugates, Inhibitors, Lectin, Multivalency
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:umu:diva-200569DOI: 10.1002/ejoc.202200795ISI: 000868847200001Scopus ID: 2-s2.0-85139931624OAI: oai:DiVA.org:umu-200569DiVA, id: diva2:1707292
Available from: 2022-10-31 Created: 2022-10-31 Last updated: 2023-01-11Bibliographically approved

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Behren, SandraWesterlind, Ulrika

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