Photoactive ligands probing the sweet taste receptor. Design and synthesis of highly potent diazirinyl D-phenylalanine derivatives

Bioorg Med Chem Lett. 2010 Feb 1;20(3):1081-3. doi: 10.1016/j.bmcl.2009.12.029. Epub 2009 Dec 11.

Abstract

Some D-amino acids such as d-tryptophan and D-phenylalanine are well known as naturally-occurring sweeteners. Photoreactive D-phenylalanine derivatives containing trifluoromethyldiazirinyl moiety at 3- or 4-position of phenylalanine, were designed as sweeteners for functional analysis with photoaffinity labeling. The trifluoromethyldiazirinyl D-phenylalanine derivatives were prepared effectively with chemo-enzymatic methods using L-amino acid oxidase and were found to have potent activity toward the human sweet taste receptor.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Crystallography, X-Ray
  • Humans
  • Phenylalanine / chemical synthesis*
  • Phenylalanine / metabolism*
  • Photoaffinity Labels / chemical synthesis*
  • Photoaffinity Labels / metabolism*
  • Protein Structure, Tertiary
  • Receptors, G-Protein-Coupled / chemistry
  • Receptors, G-Protein-Coupled / metabolism*
  • Sweetening Agents / metabolism
  • Taste Buds / chemistry
  • Taste Buds / metabolism*

Substances

  • Photoaffinity Labels
  • Receptors, G-Protein-Coupled
  • Sweetening Agents
  • taste receptors, type 1
  • Phenylalanine