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Dimerization and antidepressant recognition at noradrenaline transporter.
Zhang, Heng; Yin, Yu-Ling; Dai, Antao; Zhang, Tianwei; Zhang, Chao; Wu, Canrong; Hu, Wen; He, Xinheng; Pan, Benxun; Jin, Sanshan; Yuan, Qingning; Wang, Ming-Wei; Yang, Dehua; Xu, H Eric; Jiang, Yi.
Affiliation
  • Zhang H; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • Yin YL; Lingang Laboratory, Shanghai, China.
  • Dai A; State Key Laboratory of Chemical Biology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • Zhang T; National Center for Drug Screening, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • Zhang C; Lingang Laboratory, Shanghai, China.
  • Wu C; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
  • Hu W; National Center for Drug Screening, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • He X; School of Pharmacy, Fudan University, Shanghai, China.
  • Pan B; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • Jin S; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • Yuan Q; Shanghai Advanced Electron Microscope Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • Wang MW; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
  • Yang D; University of Chinese Academy of Sciences, Beijing, China.
  • Xu HE; Lingang Laboratory, Shanghai, China.
  • Jiang Y; Lingang Laboratory, Shanghai, China.
Nature ; 630(8015): 247-254, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38750358
ABSTRACT
The noradrenaline transporter has a pivotal role in regulating neurotransmitter balance and is crucial for normal physiology and neurobiology1. Dysfunction of noradrenaline transporter has been implicated in numerous neuropsychiatric diseases, including depression and attention deficit hyperactivity disorder2. Here we report cryo-electron microscopy structures of noradrenaline transporter in apo and substrate-bound forms, and as complexes with six antidepressants. The structures reveal a noradrenaline transporter dimer interface that is mediated predominantly by cholesterol and lipid molecules. The substrate noradrenaline binds deep in the central binding pocket, and its amine group interacts with a conserved aspartate residue. Our structures also provide insight into antidepressant recognition and monoamine transporter selectivity. Together, these findings advance our understanding of noradrenaline transporter regulation and inhibition, and provide templates for designing improved antidepressants to treat neuropsychiatric disorders.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Norepinephrine / Cryoelectron Microscopy / Norepinephrine Plasma Membrane Transport Proteins / Protein Multimerization / Antidepressive Agents Limits: Humans Language: En Journal: Nature Year: 2024 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Norepinephrine / Cryoelectron Microscopy / Norepinephrine Plasma Membrane Transport Proteins / Protein Multimerization / Antidepressive Agents Limits: Humans Language: En Journal: Nature Year: 2024 Type: Article Affiliation country: China