Development of Fluorescent Probes that Target Serotonin 5-HT2B Receptors

Sci Rep. 2017 Sep 7;7(1):10765. doi: 10.1038/s41598-017-11370-2.

Abstract

Some 5-HT2B fluorescent probes were obtained by tagging 1-(2,5-dimethoxy-4-iodophenyl)-propan-2-amine (DOI) with a subset of fluorescent amines. Some of the resulting fluorescent ligands showed excellent affinity and selectivity profiles at the 5-HT2B receptors (e.g. 12b), while retain the agonistic functional behaviour of the model ligand (DOI). The study highlighted the most salient features of the structure-activity relationship in this series and these were substantiated by a molecular modelling study based on a receptor-driven docking model constructed on the basis of the crystal structure of the human 5-HT2B receptor. One of the fluorescent ligands developed in this work, compound 12i, specifically labelled CHO-K1 cells expressing 5-HT2B receptors and not parental CHO-K1 cells in a concentration-dependent manner. 12i enables imaging and quantification of specific 5-HT2B receptor labelling in live cells by automated fluorescence microscopy as well as quantification by measurements of fluorescence intensity using a fluorescence plate reader.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzene Derivatives / chemical synthesis
  • Benzene Derivatives / chemistry*
  • CHO Cells
  • Cricetulus
  • Fluorescent Dyes / chemical synthesis
  • Fluorescent Dyes / chemistry*
  • Humans
  • Ligands
  • Microscopy, Fluorescence / methods
  • Models, Molecular
  • Molecular Docking Simulation
  • Propylamines / chemical synthesis
  • Propylamines / chemistry*
  • Receptor, Serotonin, 5-HT2B / chemistry*
  • Receptor, Serotonin, 5-HT2B / metabolism
  • Serotonin 5-HT2 Receptor Agonists / chemistry
  • Structure-Activity Relationship

Substances

  • Benzene Derivatives
  • Fluorescent Dyes
  • Ligands
  • Propylamines
  • Receptor, Serotonin, 5-HT2B
  • Serotonin 5-HT2 Receptor Agonists