Unprecedented Affinity Labeling of Carbohydrate-Binding Proteins with
Journal
Bioconjugate chemistry
ISSN: 1520-4812
Titre abrégé: Bioconjug Chem
Pays: United States
ID NLM: 9010319
Informations de publication
Date de publication:
18 09 2019
18 09 2019
Historique:
pubmed:
14
8
2019
medline:
2
9
2020
entrez:
13
8
2019
Statut:
ppublish
Résumé
Carbohydrate-protein interactions trigger a wide range of biological signaling pathways, the mainstays of physiological and pathological processes. However, there are an incredible number of carbohydrate-binding proteins (CBPs) that remain to be identified and characterized. This study reports for the first time the covalent labeling of CBPs by triazinyl glycosides, a new and promising class of affinity-based glycoprobes. Mono- and bis-clickable triazinyl glycosides were efficiently synthesized from unprotected oligosaccharides (chitinpentaose and 2'-fucosyl-lactose) in a single step. These molecules allow the specific covalent labeling of chitin-oligosaccharide-binding proteins (wheat germ agglutinin WGA and
Identifiants
pubmed: 31403275
doi: 10.1021/acs.bioconjchem.9b00432
doi:
Substances chimiques
Glycosides
0
Receptors, Cell Surface
0
Triazines
0
saccharide-binding proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM