Parallel solid-phase synthesis of mucin-like glycopeptides

Mian Liu, George Barany, David Live

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24 Scopus citations


The glycopeptide, Ac-Pro-Thr(α-d-GalNAc)-Thr(α-d-GalNAc)- Thr(α-d-GalNAc)-Pro-Leu-Lys-NH2 (1), which features three consecutive O-glycosylated Thr residues and mimics a portion of mucin 2, has been prepared by solid-phase synthesis. Seven related, partially glycosylated peptides (2-8) were synthesized as well. This suite of molecules allowed a systematic analysis of synthetic protocols. Nα-(9- Fluorenylmethoxycarbonyl)-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-d- galactopyranosyl)-l-threonine pentafluorophenyl ester [Fmoc-l-Thr(Ac 3-α-d-GalN3)-OPfp] was used as a building block that coupled efficiently when used in a relatively low molar excess, that is, ∼1.5 equiv, with N,N-dimethylformamide (DMF) as the solvent. For conversion of the azido group to the N-acetyl function, direct treatment with thioacetic acid was preferred over a two-step procedure involving reduction with dithiothreitol (DTT) followed by N-acetylation. Effective O-deacetylation of 1-8 in solution was achieved by treatment with sodium methoxide (10-15 mM; ∼5 equiv) in methanol. On-resin deacetylation techniques were also examined, using sodium methoxide (6-10 mM) in DMF-methanol (17:3) (for 4 and 11) or hydrazine (70 mM) in methanol (for 8). The more convenient on-resin technique in DMF-methanol gave yields similar to solution conditions, and promises to be widely useful for solid-phase glycopeptide synthesis. HPLC profiles showed that free glycopeptides elute earlier than the corresponding O-acetylated derivatives, and that retention times vary systematically with the number of sugar moieties. 1H NMR studies carried out in water showed an increase in conformational organization of glycopeptides with increased density of glycosylation.

Original languageEnglish (US)
Pages (from-to)2111-2122
Number of pages12
JournalCarbohydrate Research
Issue number13
StatePublished - Sep 26 2005

Bibliographical note

Funding Information:
The authors would like to thank Dr. Daniel G. Mullen for valuable technical advice and for critical reading of the manuscript, and Professor Gary R. Gray for useful suggestions. This work was supported by grant GM 66148 from the National Institutes of Health.


  • Azido functional group
  • Deacetylation
  • Glycopeptide
  • Nuclear magnetic resonance
  • Sodium methoxide
  • Solid-phase glycopeptide synthesis
  • Thioacetic acid


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