Neurotensin Receptor Allosterism Revealed in Complex with a Biased Allosteric Modulator

作者：B. Krumm, Jeffrey F. DiBerto, Reid H. J. Olsen, Hye Jin Kang, Samuel T. Slocum, Shicheng Zhang, Ryan T. Strachan, Xi‐Ping Huang, Lauren M. Slosky, Anthony B. Pinkerton, Lawrence S Barak, Marc G. Caron, Terry Kenakin, Jonathan F. Fay, Bryan L. Roth · 发表于：Biochemistry · 年份：2023 · DOI：10.1021/acs.biochem.3c00029 · 被引用次数：79 · 研究领域：Receptor Mechanisms and Signaling、Neuropeptides and Animal Physiology、Monoclonal and Polyclonal Antibodies Research

The NTSR1 neurotensin receptor (NTSR1) is a G protein-coupled receptor (GPCR) found in the brain and peripheral tissues with neurotensin (NTS) being its endogenous peptide ligand. In the brain, NTS modulates dopamine neuronal activity, induces opioid-independent analgesia, and regulates food intake. Recent studies indicate that biasing NTSR1 toward β-arrestin signaling can attenuate the actions of psychostimulants and other drugs of abuse. Here, we provide the cryoEM structures of NTSR1 ternary complexes with heterotrimeric Gq and GoA with and without the brain-penetrant small-molecule SBI-553. In functional studies, we discovered that SBI-553 displays complex allosteric actions exemplified by negative allosteric modulation for G proteins that are Gα subunit selective and positive allosteric modulation and agonism for β-arrestin translocation at NTSR1. Detailed structural analysis of the allosteric binding site illuminated the structural determinants for biased allosteric modulation of SBI-553 on NTSR1.