Glycosylation of peptides using glycosyl phosphite reagents
AssigneeThe Scripps Research Institute
InventorsChi-Huey Wong, Hirosato Kondo
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Abstract
A method for synthesizing glycosylated peptides employs a blocked carbohydrate donor and a blocked peptide acceptor. The carbohydrate donor includes an acid labile phosphite leaving group attached to the anomeric carbon. The blocked peptide acceptor includes an unprotected hydroxyl group susceptible to electrophilic attack. Serine hydroxyl is preferred. The reaction is initiated by the addition of a Lewis acid so as to activate the acid labile phosphite leaving group on the carbohydrate donor. The substitution reaction may be conducted at -78.degree. C. in a solvent such as Et.sub.3 N which favors the formation of glycosylated peptide products.
Claims5
A method for glycosylating peptides comprising the following steps:
- Step A:
- providing a blocked carbohydrate donor having an anomeric carbon with an acid labile phosphite leaving group attached thereto;
- Step B:
- blocking a peptide for providing a blocked peptide acceptor including an amino acid residue having an unprotected hydroxyl group, the amino acid residue being selected from a group consisting of serine, threonine, hydroxylysine, hydroxyproline, and hydroxyl containing pseudopeptides;
- Step C:
- providing a promotor having Lewis acid activity for catalyzing the phosphite leaving group of said Step A;
- then
- Step D:
- reacting the blocked carbohydrate donor of said Step A with the blocked peptide acceptor of said Step B in the presence of the promotor of said Step C within a solvent favoring the formation of glycosylated peptide products;
- and then
- Step E:
- quenching the reaction of said Step D.
Dependencies are inferred from the claim text.