Cellular Thermal Shift Assay for the Detection of Small Molecule-Target Interactions in Arabidopsis Cells

Methods Mol Biol. 2023:2554:21-34. doi: 10.1007/978-1-0716-2624-5_3.

Abstract

Chemical genetics takes advantage of small molecule-protein interactions to explore various biological processes. Although an attractive alternative to classical genetics in plants, the identification of small-molecule targets remains a challenge and limits the broad use of the compounds. The cellular thermal shift assay (CETSA), based on the principle that binding of small molecules could affect the thermal stability of proteins, has been applied for target validation in plant cells. Combined with high-resolution mass spectrometry, CETSA can detect small-molecule targets by monitoring the changes in the protein thermal stability caused by the interactions with small molecules at the proteome level. Here we describe the small-molecule target validation as well as the target identification with mass spectrometry by means of CETSA.

Keywords: Cellular thermal shift assay; Chemical genetics; Small-molecule target identification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis* / metabolism
  • Mass Spectrometry
  • Protein Stability
  • Proteome* / metabolism

Substances

  • Proteome