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Updated: Aug 29, 2025

Monitoring GPCR-β-arrestin1/2 Interactions in Real Time Living Systems to Accelerate Drug Discovery
Published on: June 28, 2019
Structural snapshot of a β-arrestin-biased receptor
Parishmita Sarma1, Ramanuj Banerjee1, Arun K Shukla1
1Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India.
None:
Atypical chemokine receptor subtype 3 (ACKR3), a chemokine receptor, couples selectively to β-arrestins (βarrs) but not to G proteins despite having seven transmembrane (7TM) helix architecture. Yen et al. present cryogenic-electron microscopy (cryo-EM) structures of agonist-bound ACKR3, elucidating a distinct chemokine-binding mechanism, and offering a structural template to probe the transducer-coupling bias at this receptor.
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