变构调节
变构调节剂
化学
神经降压素
异三聚体G蛋白
G蛋白偶联受体
受体
神经降压素受体
G蛋白
蛋白质亚单位
生物化学
细胞生物学
生物物理学
神经肽
生物
基因
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
出处
期刊:Biochemistry
[American Chemical Society]
日期:2023-03-14
卷期号:62 (7): 1233-1248
被引量:38
标识
DOI:10.1021/acs.biochem.3c00029
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI