Third-Party bioluminescence resonance energy transfer indicates constitutive association of membrane proteins: Application to class A G-protein-coupled receptors and G-proteins

Sudhakiranmayi Kuravi, Tien Hung Lan, Arnab Barik, Nevin A Lambert

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Many of the molecules that mediate G-protein signaling are thought to constitutively associate with each other in variably stable signaling complexes. Much of the evidence for signaling complexes has come from Förster resonance energy transfer and bioluminescence resonance energy transfer (BRET) studies. However, detection of constitutive protein association with these methods is hampered by nonspecific energy transfer that occurs when donor and acceptor molecules are in close proximity by chance. We show that chemically-induced recruitment of local third-party BRET donors or acceptors reliably separates nonspecific and specific BRET. We use this method to reexamine the constitutive association of class A G-protein-coupled receptors (GPCRs) with other GPCRs and with heterotrimeric G-proteins. We find that β2 adrenoreceptors constitutively associate with each other and with several other class A GPCRs. In contrast, GPCRs and G-proteins are unlikely to exist in stable constitutive preassembled complexes.

Original languageEnglish (US)
Pages (from-to)2383-2390
Number of pages8
JournalBiophysical Journal
Volume98
Issue number10
DOIs
StatePublished - May 19 2010

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Energy Transfer
G-Protein-Coupled Receptors
GTP-Binding Proteins
Membrane Proteins
Heterotrimeric GTP-Binding Proteins
Proteins

ASJC Scopus subject areas

  • Biophysics

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Third-Party bioluminescence resonance energy transfer indicates constitutive association of membrane proteins : Application to class A G-protein-coupled receptors and G-proteins. / Kuravi, Sudhakiranmayi; Lan, Tien Hung; Barik, Arnab; Lambert, Nevin A.

In: Biophysical Journal, Vol. 98, No. 10, 19.05.2010, p. 2383-2390.

Research output: Contribution to journalArticle

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