Quantification of ligand binding to G-protein coupled receptors on cell membranes by ellipsometry

PLoS One. 2012;7(9):e46221. doi: 10.1371/journal.pone.0046221. Epub 2012 Sep 26.

Abstract

G-protein-coupled receptors (GPCRs) are prime drug targets and targeted by approximately 60% of current therapeutic drugs such as β-blockers, antipsychotics and analgesics. However, no biophysical methods are available to quantify their interactions with ligand binding in a native environment. Here, we use ellipsometry to quantify specific interactions of receptors within native cell membranes. As a model system, the GPCR-ligand CXCL12α and its receptor CXCR4 are used. Human-derived Ishikawa cells were deposited onto gold coated slides via Langmuir-Schaefer film deposition and interactions between the receptor CXCR4 on these cells and its ligand CXCL12α were detected via total internal reflection ellipsometry (TIRE). This interaction could be inhibited by application of the CXCR4-binding drug AMD3100. Advantages of this approach are that it allows measurement of interactions in a lipid environment without the need for labelling, protein purification or reconstitution of membrane proteins. This technique is potentially applicable to a wide variety of cell types and their membrane receptors, providing a novel method to determine ligand or drug interactions targeting GPCRs and other membrane proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzylamines
  • Cell Line
  • Cell Membrane / genetics
  • Cell Membrane / metabolism*
  • Chemokine CXCL12 / genetics
  • Chemokine CXCL12 / metabolism
  • Cyclams
  • Heterocyclic Compounds / pharmacology
  • Humans
  • Immunoblotting
  • Microscopy, Confocal
  • Protein Binding / drug effects
  • Receptors, CXCR / genetics
  • Receptors, CXCR / metabolism*
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / metabolism*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • ACKR3 protein, human
  • Benzylamines
  • CXCL12 protein, human
  • CXCR4 protein, human
  • Chemokine CXCL12
  • Cyclams
  • Heterocyclic Compounds
  • Receptors, CXCR
  • Receptors, CXCR4
  • Receptors, G-Protein-Coupled
  • plerixafor