| Literature DB >> 32744401 |
Blijke S Kroezen1, Gabriele Conti1, Benedetta Girardi1, Jonathan Cramer1, Xiaohua Jiang1, Said Rabbani1, Jennifer Müller1, Maja Kokot1, Enrico Luisoni1, Daniel Ricklin1, Oliver Schwardt1, Beat Ernst1.
Abstract
Siglecs are members of the immunoglobulin gene family containing sialic acid binding N-terminal domains. Among them, Siglec-8 is expressed on various cell types of the immune system such as eosinophils, mast cells and weakly on basophils. Cross-linking of Siglec-8 with monoclonal antibodies triggers apoptosis in eosinophils and inhibits degranulation of mast cells, making Siglec-8 a promising target for the treatment of eosinophil- and mast cell-associated diseases such as asthma. The tetrasaccharide 6'-sulfo-sialyl Lewisx has been identified as a specific Siglec-8 ligand in glycan array screening. Here, we describe an extended study enlightening the pharmacophores of 6'-sulfo-sialyl Lewisx and the successful development of a high-affinity mimetic. Retaining the neuraminic acid core, the introduction of a carbocyclic mimetic of the Gal moiety and a sulfonamide substituent in the 9-position gave a 20-fold improved binding affinity. Finally, the residence time, which usually is the Achilles tendon of carbohydrate/lectin interactions, could be improved.Entities:
Keywords: 6’-sulfo-sialyl Lewisx; Siglec-8; asthma; calorimetry; glycosides
Year: 2020 PMID: 32744401 DOI: 10.1002/cmdc.202000417
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466