Discovery of a Broad-Spectrum Fluorogenic Agonist for Strigolactone Receptors through a Computational Approach

J Agric Food Chem. 2021 Sep 15;69(36):10486-10495. doi: 10.1021/acs.jafc.1c03471. Epub 2021 Sep 3.

Abstract

Strigolactones (SLs) are plant hormones that play various roles in plant physiology, including provoking the germination of parasitic weeds Orobanche and Striga. A family of α/β-hydrolases have been proposed to be the SL receptor proteins. Effective assays for measuring the activity of SL receptors could promote the development of SL-related biology and chemistry. In this study, we developed a new approach called pharmacophore-linked probe virtual screening (PPVS). Its application yielded an effective "off-on" probe named Xilatone Red (XLR). This probe showed a broad spectrum and excellent sensitivity toward SL receptors, including ShD14 (Striga D14), for which the detection limit was determined to be in the micromolar range, outperforming that of the commercial fluorogenic agonist Yoshimulactone Green (YLG). Upon hydrolysis by SL receptors, XLR provided fluorogenic and colorimetric signaling responses. Furthermore, XLR could induce germination of Phelipanche aegyptiaca seeds and prevent Arabidopsis max4-1 branching defects at micromolar concentrations. Our molecular simulations revealed the essential factors in the molecular perception of XLR. We anticipate that this study can prompt the discovery of high-performance SL agonists/antagonists to combat parasitic weeds.

Keywords: computational discovery; fluorogenic substrate; strigolactone; strigolactone receptor; strigolactone-like bioactivity.

MeSH terms

  • Germination
  • Heterocyclic Compounds, 3-Ring
  • Lactones
  • Orobanche*
  • Striga*

Substances

  • GR24 strigolactone
  • Heterocyclic Compounds, 3-Ring
  • Lactones