Molecular Mechanisms of Methamphetamine-Induced Addiction via TAAR1 Activation

Trace amine-associated receptor 1 (TAAR1), a member of the trace amine receptor family, recognizes various trace amines in the brain, including endogenous β-phenylethylamine (PEA) and methamphetamine (METH). TAAR1 is a novel target for several neurological disorders, including schizophrenia, depression, and substance abuse. Herein, we report the structure of the human TAAR1-G<sub>s</sub> protein complex bound to METH. Using functional studies, we reveal the molecular basis of METH recognition by TAAR1, and potential mechanisms underlying the selectivity of TAAR1 for different ligands. Molecular dynamics simulations further elucidated possible mechanisms for the binding of chiral amphetamine (AMPH)-like psychoactive drugs to TAAR1. Additionally, we discovered a hydrophobic core on the transmembrane helices (TM), TM5 and TM6, explaining the unique mechanism of TAAR1 activation. These findings reveal the ligand recognition pattern and activation mechanism of TAAR1, which has important implications for the development of next-generation treatments for substance abuse and various neurological disorders.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2024-10-02
DOI
https://doi.org/10.1021/acs.jmedchem.4c01961
Citations
7
Primary Topic
Receptor Mechanisms and Signaling
Type
article
Field-Weighted Citation Impact
1.64

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article

Molecular Mechanisms of Methamphetamine-Induced Addiction via TAAR1 Activation

Fan Shi, Linlin Yang, Anna Qiao, Shan Wu et al.
7 citations
Journal of Medicinal Chemistry
Receptor Mechanisms and Signaling
1.64
article

Molecular Mechanisms of Methamphetamine-Induced Addiction via TAAR1 Activation

Fan Shi, Linlin Yang, Anna Qiao, Shan Wu, Jiening Wang, Sheng Ye, Yun Lin
article en
7 citations

Abstract

Trace amine-associated receptor 1 (TAAR1), a member of the trace amine receptor family, recognizes various trace amines in the brain, including endogenous β-phenylethylamine (PEA) and methamphetamine (METH). TAAR1 is a novel target for several neurological disorders, including schizophrenia, depression, and substance abuse. Herein, we report the structure of the human TAAR1-G<sub>s</sub> protein complex bound to METH. Using functional studies, we reveal the molecular basis of METH recognition by TAAR1, and potential mechanisms underlying the selectivity of TAAR1 for different ligands. Molecular dynamics simulations further elucidated possible mechanisms for the binding of chiral amphetamine (AMPH)-like psychoactive drugs to TAAR1. Additionally, we discovered a hydrophobic core on the transmembrane helices (TM), TM5 and TM6, explaining the unique mechanism of TAAR1 activation. These findings reveal the ligand recognition pattern and activation mechanism of TAAR1, which has important implications for the development of next-generation treatments for substance abuse and various neurological disorders.

Journal of Medicinal ChemistryVol. 67(20)
Tianjin University (CN), Zhengzhou University (CN), Hubei University (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Fundamental Research Funds for the Central Universities
Good health and well-being
Openalex Percentile: Top 16%
Receptor Mechanisms and Signaling
1.64
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