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        Understanding the LigandReceptorG Protein Ternary Complex for GPCR Drug Discovery

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        Understanding the ternary complex between G protein-coupled receptors (GPCRs), cognate G proteins, and their ligands is an important landmark for drug discovery. Yet, little is known about the specific interactions between GPCRs and G proteins. For a better perspective on the ternary complex dynamics, we adapted a β2 -adrenergic receptor(β2 AR)–tetGsα reconstitution system and found evidence that for efficient coupling of the β2 AR to Gs does not require specific interactions between the βγ-subunits and the β2 AR. Our results demonstrate that specific interactions between βγ and the β2 AR are not required for G protein activation but likely serve to anchor Gsα to the plasma membrane. Our results also suggests that the advantages of analysis of G protein activation by using β2 AR receptor–tetGsα system in vitro at the close proximity of the receptor may constitute a simple screening system that avoids false positives and potentially adapted to screen drugs for other GPCRs.
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