Identification of ABA Receptor Agonists Using a Multiplexed High-Throughput Chemical Screening

Methods Mol Biol. 2021:2213:99-111. doi: 10.1007/978-1-0716-0954-5_9.

Abstract

Small molecules that can activate abscisic acid (ABA) receptors represent valuable probes to study ABA perception and signaling. Additionally, these compounds have the potential to be used in the field to counteract the negative effect of drought stress on plant productivity. The PYR/PYL ABA receptors, in their ligand-bound conformation, inactivate protein phosphatases 2C (PP2Cs), triggering physiological responses that are essential for plant adaptation to environmental stresses, including drought. Based on this ligand-induced PP2C inactivation mechanism, we have developed an in vitro assay for the identification of ABA-receptor agonists by high-throughput screening of chemical libraries. The assay allows simultaneous use of different ABA receptors, increasing the chances to find new agonists and eliminates the need for parallel screening. In this chapter, we describe detailed procedures for the identification of ABA agonists using this multiplexed assay in a medium- (96-well plates) or a high-throughput (384-well plates) setup.

Keywords: Abscisic acid; Agonist; Chemical genomics; Drought; High-throughput; PP2C; Plant; Screening; Small molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abscisic Acid / metabolism*
  • Arabidopsis Proteins / isolation & purification
  • Enzyme Assays
  • High-Throughput Screening Assays / methods*
  • Protein Phosphatase 2C / metabolism
  • Receptors, Cell Surface / agonists*
  • Receptors, Cell Surface / metabolism
  • Signal Transduction
  • Small Molecule Libraries / analysis*

Substances

  • Arabidopsis Proteins
  • Receptors, Cell Surface
  • Small Molecule Libraries
  • Abscisic Acid
  • Protein Phosphatase 2C