Chemo-enzymatic synthesis of a glycosylated peptide containing a complex N-glycan based on unprotected oligosaccharides by using DMT-MM and Endo-M

For chemo-enzymatic synthesis of a glycosylated peptide, 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) was used for the synthesis of a N -acetylglucosaminyl peptide and a pseudoglycopeptide by solid-phase peptide synthesis without the requirement of protecting groups on...

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Veröffentlicht in:Glycoconjugate journal 2017-08, Vol.34 (4), p.481-487
Hauptverfasser: Tomabechi, Yusuke, Katoh, Toshihiko, Kunishima, Munetaka, Inazu, Toshiyuki, Yamamoto, Kenji
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Sprache:eng
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Zusammenfassung:For chemo-enzymatic synthesis of a glycosylated peptide, 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) was used for the synthesis of a N -acetylglucosaminyl peptide and a pseudoglycopeptide by solid-phase peptide synthesis without the requirement of protecting groups on the carbohydrate. We also performed transglycosylation of an N-glycan to the N -acetylglucosaminyl peptide using endo-β- N -acetylglucosaminidase from Mucor hiemalis (Endo-M) to synthesize a glycopeptide containing a complex N-glycan.
ISSN:0282-0080
1573-4986
DOI:10.1007/s10719-017-9770-y