Allosteric "beta-blocker" isolated from a DNA-encoded small molecule library.

Journal Article (Journal Article)

The β2-adrenergic receptor (β2AR) has been a model system for understanding regulatory mechanisms of G-protein-coupled receptor (GPCR) actions and plays a significant role in cardiovascular and pulmonary diseases. Because all known β-adrenergic receptor drugs target the orthosteric binding site of the receptor, we set out to isolate allosteric ligands for this receptor by panning DNA-encoded small-molecule libraries comprising 190 million distinct compounds against purified human β2AR. Here, we report the discovery of a small-molecule negative allosteric modulator (antagonist), compound 15 [([4-((2S)-3-(((S)-3-(3-bromophenyl)-1-(methylamino)-1-oxopropan-2-yl)amino)-2-(2-cyclohexyl-2-phenylacetamido)-3-oxopropyl)benzamide], exhibiting a unique chemotype and low micromolar affinity for the β2AR. Binding of 15 to the receptor cooperatively enhances orthosteric inverse agonist binding while negatively modulating binding of orthosteric agonists. Studies with a specific antibody that binds to an intracellular region of the β2AR suggest that 15 binds in proximity to the G-protein binding site on the cytosolic surface of the β2AR. In cell-signaling studies, 15 inhibits cAMP production through the β2AR, but not that mediated by other Gs-coupled receptors. Compound 15 also similarly inhibits β-arrestin recruitment to the activated β2AR. This study presents an allosteric small-molecule ligand for the β2AR and introduces a broadly applicable method for screening DNA-encoded small-molecule libraries against purified GPCR targets. Importantly, such an approach could facilitate the discovery of GPCR drugs with tailored allosteric effects.

Full Text

Duke Authors

Cited Authors

  • Ahn, S; Kahsai, AW; Pani, B; Wang, Q-T; Zhao, S; Wall, AL; Strachan, RT; Staus, DP; Wingler, LM; Sun, LD; Sinnaeve, J; Choi, M; Cho, T; Xu, TT; Hansen, GM; Burnett, MB; Lamerdin, JE; Bassoni, DL; Gavino, BJ; Husemoen, G; Olsen, EK; Franch, T; Costanzi, S; Chen, X; Lefkowitz, RJ

Published Date

  • February 14, 2017

Published In

Volume / Issue

  • 114 / 7

Start / End Page

  • 1708 - 1713

PubMed ID

  • 28130548

Pubmed Central ID

  • PMC5321036

Electronic International Standard Serial Number (EISSN)

  • 1091-6490

Digital Object Identifier (DOI)

  • 10.1073/pnas.1620645114


  • eng

Conference Location

  • United States