Monitoring Ligand-Activated Protein-Protein Interactions Using Bioluminescent Resonance Energy Transfer (BRET) Assay

Methods Mol Biol. 2016:1473:3-15. doi: 10.1007/978-1-4939-6346-1_1.

Abstract

The bioluminescent resonance energy transfer (BRET) assay has been extensively used in cell-based and in vivo imaging systems for detecting protein-protein interactions in the native environment of living cells. These protein-protein interactions are essential for the functional response of many signaling pathways to environmental chemicals. BRET has been used as a toxicological tool for identifying chemicals that either induce or inhibit these protein-protein interactions. This chapter focuses on describing the toxicological applications of BRET and its optimization as a high-throughput detection system in live cells. Here we review the construction of BRET fusion proteins, describe the BRET methodology, and outline strategies to overcome obstacles that may arise. Furthermore, we describe the advantage of BRET over other resonance energy transfer methods for monitoring protein-protein interactions.

Keywords: Bioluminescent Resonance Energy Transfer (BRET); Imaging assay; Protein–protein interactions; Screening assay.

Publication types

  • Review

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bioluminescence Resonance Energy Transfer Techniques*
  • Endocrine Disruptors / toxicity*
  • Estrogen Receptor alpha / genetics*
  • Estrogen Receptor alpha / metabolism
  • Estrogen Receptor beta / genetics*
  • Estrogen Receptor beta / metabolism
  • Gene Expression Regulation / drug effects*
  • HEK293 Cells
  • High-Throughput Screening Assays
  • Humans
  • Luciferases / genetics
  • Luciferases / metabolism
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Protein Interaction Mapping
  • Protein Multimerization / drug effects
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism

Substances

  • Bacterial Proteins
  • ESR1 protein, human
  • Endocrine Disruptors
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Luminescent Proteins
  • Recombinant Fusion Proteins
  • yellow fluorescent protein, Bacteria
  • Luciferases