Design and synthesis of AX7574: a microcystin-derived, fluorescent probe for serine/threonine phosphatases

Bioconjug Chem. 2004 Jul-Aug;15(4):790-8. doi: 10.1021/bc0499580.

Abstract

The design and synthesis of AX7574, a microcystin-derived probe for serine/threonine phosphatases, is described. A key step in the synthesis was the conjugation under basic conditions of a tetramethylrhodamine 1,3-diketone derivative to the arginine side chain present in microcystin-LR. The resulting conjugate specifically labeled the active site of protein phosphatases 1 (PP-1) with a 1:1 stoichiometry and IC50 of 4.0 nM. AX7574 was used to isolate and identify PP-1, PP-2A, PP-4, and PP-6 in Jurkat cells. Finally, AX7574 was able to record changes in the phosphatase activity levels of calyculin A treated Jurkat cells versus untreated control cells.

MeSH terms

  • Drug Design*
  • Enzyme Inhibitors / pharmacology
  • Fluorescence
  • Fluorescent Dyes
  • Humans
  • Inhibitory Concentration 50
  • Jurkat Cells
  • Kinetics
  • Marine Toxins
  • Mass Spectrometry
  • Microcystins
  • Molecular Probes / analysis*
  • Molecular Probes / antagonists & inhibitors
  • Molecular Probes / chemical synthesis*
  • Molecular Probes / chemistry
  • Molecular Structure
  • Oxazoles / pharmacology
  • Peptides, Cyclic / analysis*
  • Peptides, Cyclic / antagonists & inhibitors
  • Peptides, Cyclic / chemical synthesis*
  • Peptides, Cyclic / chemistry*
  • Phosphoprotein Phosphatases / analysis
  • Phosphoprotein Phosphatases / metabolism*
  • Proteome / drug effects
  • Proteome / metabolism
  • Staining and Labeling

Substances

  • AX 7574
  • Enzyme Inhibitors
  • Fluorescent Dyes
  • Marine Toxins
  • Microcystins
  • Molecular Probes
  • Oxazoles
  • Peptides, Cyclic
  • Proteome
  • microcystin
  • calyculin A
  • Phosphoprotein Phosphatases