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Glycosylation of Pramlintide: Synthetic Glycopeptides that Display In Vitro and In Vivo Activities as Amylin Receptor Agonists.

Chemistry.. 2013-10; 
Tomabechi Y, Krippner G, Rendle PM, Squire MA, Fairbanks AJ. Department of Chemistry, University of Canterbury, Private Bag 4800, Christchurch 8140 (New Zealand).
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摘要

Sweet medicine: Glycosylated analogues of pramlintide, in which specific Asn residues bear extended N-glycan structures, may be accessed by a combination of solid-phase peptide synthesis and highly efficient enzymatic glycosylation (see scheme; ENGases=endo-β-N-acetylglucosaminidases). Glycopeptides display both in vitro and in vivo activity as amylin receptor agonists and effect 'smoothing' of blood glucose.

关键词

carbohydrates; diabetes; enzymes; glycopeptides; pramlintide