Encouraging progress in the ω-aspartylation of complex oligosaccharides as a general route to β-N-linked glycopolypeptides

J Am Chem Soc. 2011 Feb 9;133(5):1597-602. doi: 10.1021/ja110115a. Epub 2011 Jan 5.

Abstract

Described herein is a method for the joining of complex peptides to complex oligosaccharides via an N-linkage. The ω-aspartylation is conducted by coupling fully deprotected glycosylamine with a peptide containing a unique thioacid at the ω-aspartate carboxyl. In the presence of HOBT, under conditions that, in principle, allow for oxidation, complex components are combined in encouraging yields to produce structurally and stereochemically defined N-linked glycopolypeptides wherein the carbohydrate domain can be quite complex. Various mechanisms for oxidative coupling are proposed.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amines / chemistry
  • Amino Acid Sequence
  • Aspartic Acid / chemistry*
  • Glycopeptides / chemical synthesis
  • Glycopeptides / chemistry*
  • Nitrogen / chemistry*
  • Oligosaccharides / chemistry*

Substances

  • Amines
  • Glycopeptides
  • Oligosaccharides
  • Aspartic Acid
  • Nitrogen