Supramolecular protection from the enzymatic tyrosine phosphorylation in a polypeptide

Chem Commun (Camb). 2016 Jun 21;52(52):8142-5. doi: 10.1039/c6cc03875a.

Abstract

Here we report two new artificial pseudopeptidic cages that bind the EYE peptide epitope in pure water at physiological pH (as studied by fluorescence and NMR spectroscopies). The supramolecular complexation of the Tyr residues efficiently precludes their subsequent PTK-catalysed phosphorylation. Our results show a supramolecular modulation of the PTK activity by competitive substrate caging.

MeSH terms

  • Biocatalysis
  • Macromolecular Substances / chemistry
  • Macromolecular Substances / metabolism
  • Molecular Conformation
  • Peptides / chemistry
  • Peptides / metabolism*
  • Phosphorylation
  • Protein-Tyrosine Kinases / chemistry
  • Protein-Tyrosine Kinases / metabolism*
  • Tyrosine / chemistry
  • Tyrosine / metabolism*

Substances

  • Macromolecular Substances
  • Peptides
  • Tyrosine
  • Protein-Tyrosine Kinases