Cassia obtusifolia MetE as a cytosolic target for potassium isolespedezate, a leaf-opening factor of Cassia plants: target exploration by a compact molecular-probe strategy

Chem Asian J. 2011 Dec 2;6(12):3286-97. doi: 10.1002/asia.201100392. Epub 2011 Aug 3.

Abstract

Affinity chromatography by using ligand-immobilized bead technology is generally the first choice for target exploration of a bioactive ligand. However, when a ligand has comparatively low affinity against its target, serious difficulties will be raised in affinity-based target detection. We report here that the use of compact molecular probes (CMP) will be advantageous in such cases; it enables the retention of moderate affinity between the ligand and its target in contrast to immobilizing the ligand on affinity beads that will cause a serious drop in affinity to preclude target detection. In the CMP strategy, a CMP containing an azide handle is used for an initial affinity-based labeling of target, and subsequent tagging by CuAAC with a large FLAG tag will give a tagged target protein. By using the CMP strategy, we succeeded in the identification of Cassia obtusifolia MetE as a cytosolic target protein of potassium isolespedezate (1), a moderately bioactive ligand.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cassia / enzymology*
  • Chromatography, Affinity
  • Coumaric Acids / chemistry
  • Coumaric Acids / metabolism*
  • Glucosides / chemistry
  • Glucosides / metabolism*
  • Methyltransferases / analysis
  • Methyltransferases / metabolism*
  • Molecular Probes / chemistry
  • Molecular Probes / metabolism*
  • Molecular Sequence Data
  • Plant Leaves / physiology
  • Plant Proteins / analysis
  • Plant Proteins / metabolism*
  • Sequence Alignment

Substances

  • Coumaric Acids
  • Glucosides
  • Molecular Probes
  • Plant Proteins
  • isolespedezic acid
  • Methyltransferases