Quantification of Molecular Interactions in Living Cells in Real Time using a Membrane Protein Nanopattern

Anal Chem. 2020 Jul 7;92(13):8983-8991. doi: 10.1021/acs.analchem.0c00987. Epub 2020 Jun 11.


Molecular processes within cells have traditionally been studied with biochemical methods due to their high degree of specificity and ease of use. In recent years, cell-based assays have gained more and more popularity since they facilitate the extraction of mode of action, phenotypic, and toxicity information. However, to provide specificity, cellular assays rely heavily on biomolecular labels and tags while label-free cell-based assays only offer holistic information about a bulk property of the investigated cells. Here, we introduce a cell-based assay for protein-protein interaction analysis. We achieve specificity by spatially ordering a membrane protein of interest into a coherent pattern of fully functional membrane proteins on the surface of an optical sensor. Thereby, molecular interactions with the coherently ordered membrane proteins become visible in real time, while nonspecific interactions and holistic changes within the living cell remain invisible. Due to its unbiased nature, this new cell-based detection method presents itself as an invaluable tool for cell signaling research and drug discovery.

MeSH terms

  • Arrestin / chemistry
  • Arrestin / genetics
  • Arrestin / metabolism
  • Fluorescence Resonance Energy Transfer / methods*
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • HEK293 Cells
  • Humans
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Protein Interaction Maps
  • Receptors, Adrenergic, beta-2 / chemistry
  • Receptors, Adrenergic, beta-2 / genetics
  • Receptors, Adrenergic, beta-2 / metabolism


  • Arrestin
  • Membrane Proteins
  • Receptors, Adrenergic, beta-2
  • Green Fluorescent Proteins