Receptor-Ligand Interaction Measured by Inductively Coupled Plasma Mass Spectrometry and Selenium Labeling

J Med Chem. 2018 Nov 21;61(22):10173-10184. doi: 10.1021/acs.jmedchem.8b01320. Epub 2018 Nov 8.

Abstract

In the search for an alternative strategy to the radioactivity measurement conventionally performed to probe receptor-ligand interactions in pharmacological assays, we demonstrated that selenium labeling of the studied ligand combined with elemental mass spectrometry was as efficient and robust as the reference method but devoid of its environmental and health hazards. The proof-of-concept was illustrated on two GPCR receptors, vasopressin (V1A) and cholecystokinin B (CCK-B), involving peptides as endogenous ligands. We proposed several methodologies to produce selenium-labeled ligands according to peptide sequences along with binding affinity constraints. A selection of selenopeptides that kept high affinities toward the targeted receptor were engaged in saturation and competitive binding experiments with subsequent sensitive RP-LC-ICP-MS measurements. Experimental values of affinity constant ( Ki) were perfectly correlated to literature data, illustrating the general great potency of replacing radioactive iodine by selenium for ligand labeling to further undergo unaffected pharmacology experiments efficiently monitored by elemental mass spectrometry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cricetulus
  • Isotope Labeling
  • Ligands
  • Mass Spectrometry*
  • Peptides / chemistry
  • Peptides / metabolism
  • Protein Binding
  • Receptor, Cholecystokinin B / metabolism
  • Selenium / chemistry*
  • Vasopressins / metabolism

Substances

  • Ligands
  • Peptides
  • Receptor, Cholecystokinin B
  • Vasopressins
  • Selenium