A Potent Mimetic of the Siglec-8 Ligand 6'-Sulfo-Sialyl Lewis.

ChemMedChem

Molecular Pharmacy Group Department of Pharmaceutical Sciences, University of Basel, Klingelbergstrasse 50, 4056, Basel, Switzerland.

Published: September 2020

AI Article Synopsis

  • * Targeting Siglec-8 can lead to cell death in eosinophils and reduce the activity of mast cells, making it a potential treatment method for related diseases.
  • * Researchers have developed a high-affinity mimic of a specific Siglec-8 ligand, which binds better than before, enhancing its ability to engage with the target protein effectively.

Article 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 Lewis 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 Lewis 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.

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Source
http://dx.doi.org/10.1002/cmdc.202000417DOI Listing

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