Heteromultivalent Glycooligomers as Mimetics of Blood Group Antigens

Chemistry. 2019 Mar 1;25(13):3301-3309. doi: 10.1002/chem.201804505. Epub 2019 Feb 7.

Abstract

Precision glycomacromolecules have proven to be important tools for the investigation of multivalent carbohydrate-lectin interactions by presenting multiple glycan epitopes on a highly-defined synthetic scaffold. Herein, we present a new strategy for the versatile assembly of heteromultivalent glycomacromolecules that contain different carbohydrate motifs in proximity within the side chains. A new building block suitable for the solid-phase polymer synthesis of precision glycomacromolecules was developed with a branching point in the side chain that bears a free alkyne and a TIPS-protected alkyne moiety, which enables the subsequent attachment of different carbohydrate motifs by on-resin copper-mediated azide-alkyne cycloaddition reactions. Applying this synthetic strategy, heteromultivalent glycooligomers presenting fragments of histo-blood group antigens and human milk oligosaccharides were synthesized and tested for their binding behavior towards bacterial lectin LecB.

Keywords: carbohydrates; glycomimetics; oligosaccharides; precision glycomacromolecules; solid-phase synthesis.

MeSH terms

  • Alkynes / chemical synthesis
  • Alkynes / chemistry
  • Azides / chemical synthesis
  • Azides / chemistry
  • Biomimetic Materials / chemical synthesis
  • Biomimetic Materials / chemistry*
  • Blood Group Antigens / chemistry*
  • Carbohydrates / chemical synthesis
  • Carbohydrates / chemistry*
  • Cycloaddition Reaction / methods
  • Humans
  • Milk, Human / chemistry
  • Oligosaccharides / chemical synthesis
  • Oligosaccharides / chemistry*
  • Solid-Phase Synthesis Techniques / methods*

Substances

  • Alkynes
  • Azides
  • Blood Group Antigens
  • Carbohydrates
  • Oligosaccharides