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Advances in understanding and exploiting Siglec-glycan interactions.
Jame-Chenarboo, Zeinab; Gray, Taylor E; Macauley, Matthew S.
Affiliation
  • Jame-Chenarboo Z; Department of Chemistry, University of Alberta, Canada.
  • Gray TE; Department of Chemistry, University of Alberta, Canada.
  • Macauley MS; Department of Chemistry, University of Alberta, Canada; Department of Medical Microbiology and Immunology, University of Alberta, Canada. Electronic address: macauley@ualberta.ca.
Curr Opin Chem Biol ; 80: 102454, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38631213
ABSTRACT
Sialic-acid-binding immunoglobulin-type lectins (Siglecs) are a family of cell-surface immunomodulatory receptors that recognize sialic-acid-containing glycans. The majority of Siglecs have an inhibitory motif in their intercellular domain and can regulate the cellular activation of immune cells. Importantly, the immunomodulatory role of Siglecs is regulated by engagement with distinct sialoglycan ligands. However, there are still many unanswered questions about the precise ligand(s) recognized by individual Siglec family members. New tools and approaches to study Siglec-ligand interactions are rapidly filling this knowledge gap. This review provides an overview of recent advances in discovering Siglec ligands as well as the development of approaches to modulate the function of Siglecs. In both aspects, chemical biology approaches are emphasized with a discussion on how these are complementing biochemical and genetic strategies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Sialic Acid Binding Immunoglobulin-like Lectins Limits: Animals / Humans Language: En Journal: Curr Opin Chem Biol Journal subject: BIOQUIMICA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Sialic Acid Binding Immunoglobulin-like Lectins Limits: Animals / Humans Language: En Journal: Curr Opin Chem Biol Journal subject: BIOQUIMICA Year: 2024 Document type: Article Affiliation country: Country of publication: