Targeting G Protein-Coupled Receptors with Magnetic Carbon Nanotubes: The Case of the A3 Adenosine Receptor

ChemMedChem. 2020 Oct 19;15(20):1909-1920. doi: 10.1002/cmdc.202000466. Epub 2020 Sep 8.

Abstract

The A3 adenosine receptor (AR) is a G protein-coupled receptor (GPCR) overexpressed in the membrane of specific cancer cells. Thus, the development of nanosystems targeting this receptor could be a strategy to both treat and diagnose cancer. Iron-filled carbon nanotubes (CNTs) are an optimal platform for theranostic purposes, and the use of a magnetic field can be exploited for cancer magnetic cell sorting and thermal therapy. In this work, we have conjugated an A3 AR ligand on the surface of iron-filled CNTs with the aim of targeting cells overexpressing A3 ARs. In particular, two conjugates bearing PEG linkers of different length were designed. A docking analysis of A3 AR showed that neither CNT nor linker interferes with ligand binding to the receptor; this was confirmed by in vitro preliminary radioligand competition assays on A3 AR. Encouraged by this result, magnetic cell sorting was applied to a mixture of cells overexpressing or not the A3 AR in which our compound displayed indiscriminate binding to all cells. Despite this, it is the first time that a GPCR ligand has been anchored to a magnetic nanosystem, thus it opens the door to new applications for cancer treatment.

Keywords: A3 adenosine receptors; G protein-coupled receptors; carbon nanotubes; docking; magnetic cell sorting; theranostics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cell Line, Tumor
  • Cell Separation / methods*
  • Cricetulus
  • Humans
  • Iron / chemistry
  • Magnetic Phenomena
  • Nanotubes, Carbon / chemistry*
  • Pyrazoles / chemical synthesis
  • Pyrazoles / chemistry
  • Pyrimidines / chemical synthesis
  • Pyrimidines / chemistry
  • Receptor, Adenosine A3 / metabolism*
  • Triazoles / chemical synthesis
  • Triazoles / chemistry

Substances

  • ADORA3 protein, human
  • Nanotubes, Carbon
  • Pyrazoles
  • Pyrimidines
  • Receptor, Adenosine A3
  • Triazoles
  • Iron