BRET biosensors to study GPCR biology, pharmacology, and signal transduction.

Published online

Journal Article

Bioluminescence resonance energy transfer (BRET)-based biosensors have been extensively used over the last decade to study protein-protein interactions and intracellular signal transduction in living cells. In this review, we discuss the various BRET biosensors that have been developed to investigate biology, pharmacology, and signaling of G protein-coupled receptors (GPCRs). GPCRs form two distinct types of multiprotein signal transduction complexes based upon their inclusion of G proteins or β-arrestins that can be differentially affected by drugs that exhibit functional selectivity toward G protein or β-arrestin signaling. BRET has been especially adept at illuminating the dynamics of protein-protein interactions between receptors, G proteins, β-arrestins, and their many binding partners in living cells; as well as measuring the formation and accumulation of second messengers following receptor activation. Specifically, we discuss in detail the application of BRET to study dopamine and trace amine receptors signaling, presenting examples of an exchange protein activated by cAMP biosensor to measure cAMP, β-arrestin biosensors to determine β-arrestin recruitment to the receptor, and dopamine D2 receptor and trace amine-associated receptor 1 biosensors to investigate heterodimerization between them. As the biochemical spectrum of BRET biosensors expands, the number of signaling pathways that can be measured will concomitantly increase. This will be particularly useful for the evaluation of functional selectivity in which the real-time BRET capability to measure distinct signaling modalities will dramatically shorten the time to characterize new generation of biased drugs. These emerging approaches will further expand the growing application of BRET in the screening for novel pharmacologically active compounds.

Full Text

Duke Authors

Cited Authors

  • Salahpour, A; Espinoza, S; Masri, B; Lam, V; Barak, LS; Gainetdinov, RR

Published Date

  • 2012

Published In

Volume / Issue

  • 3 /

Start / End Page

  • 105 -

PubMed ID

  • 22952466

Pubmed Central ID

  • 22952466

Electronic International Standard Serial Number (EISSN)

  • 1664-2392

Digital Object Identifier (DOI)

  • 10.3389/fendo.2012.00105

Language

  • eng

Conference Location

  • Switzerland