Structurally diverse disaccharide analogs of antifreeze glycoproteins and their ability to inhibit ice recrystallization

Bioorg Med Chem Lett. 2012 Feb 15;22(4):1719-21. doi: 10.1016/j.bmcl.2011.12.097. Epub 2011 Dec 30.

Abstract

The β-d-galactosyl-(1,3)-α-N-acetyl-d-galactosamine disaccharide is present in antifreeze glycoproteins (AFGPs). Analogs of this disaccharide including the β-linked (1,3)-, (1,4)-, and (1,6)-galactosyl-N-acetyl galactosamine and the β-(1,3)-galactosyl-galactoside were synthesized and evaluated for ice recrystallization inhibition (IRI) activity. The results from this study demonstrate that the β-linked-(1,4) disaccharide exhibits more potent IRI activity than the native β-linked-(1,3) disaccharide. The C2 N-acetyl group of the disaccharide does not affect IRI activity but in monosaccharides, the presence of the C2 N-acetyl group decreases IRI activity. The current study will facilitate the design of potent small-molecule ice recrystallization inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifreeze Proteins / chemistry*
  • Crystallization
  • Disaccharides / chemistry*
  • Molecular Structure

Substances

  • Antifreeze Proteins
  • Disaccharides