Molecular basis of human noradrenaline transporter reuptake and inhibition

• 成果类型: Article
• 署名作者: Tan, Jiaxin; Xiao, Yuan; Kong, Fang; Zhang, Xiaochun; Xu, Hanwen; Zhu, Angqi; Liu, Yiming; Lei, Jianlin; Tian, Boxue; Yuan, Yafei; Yan, Chuangye
• 署名单位: Tsinghua University; Tsinghua University
• 刊物名称: Nature
• ISSN/ISSBN: 0028-6367
• DOI: 10.1038/s41586-024-07719-z
• 发表日期: 2024-08-22
• 关键词: x-ray structures; human serotonin; prefrontal cortex; structural basis; diverse antidepressants; monoamine transporters; dopamine transporter; bacterial homolog; cryo-em; neurotransmitter

摘要

Noradrenaline, also known as norepinephrine, has a wide range of activities and effects on most brain cell types1. Its reuptake from the synaptic cleft heavily relies on the noradrenaline transporter (NET) located in the presynaptic membrane2. Here we report the cryo-electron microscopy (cryo-EM) structures of the human NET in both its apo state and when bound to substrates or antidepressant drugs, with resolutions ranging from 2.5 & Aring; to 3.5 & Aring;. The two substrates, noradrenaline and dopamine, display a similar binding mode within the central substrate binding site (S1) and within a newly identified extracellular allosteric site (S2). Four distinct antidepressants, namely, atomoxetine, desipramine, bupropion and escitalopram, occupy the S1 site to obstruct substrate transport in distinct conformations. Moreover, a potassium ion was observed within sodium-binding site 1 in the structure of the NET bound to desipramine under the KCl condition. Complemented by structural-guided biochemical analyses, our studies reveal the mechanism of substrate recognition, the alternating access of NET, and elucidate the mode of action of the four antidepressants. The cryo-electron microscopy structures of the human noradrenaline transporter in both the apo state and bound to substrates or antidepressant drugs are resolved.