对α6β4尼古丁乙胆受体功能和连接体识别的分子洞察
Jiawei Su1,2,3, Zhuoya Yu1,2,3, Zhengji Yin4,5
1National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Nature communications
|April 2, 2025
概括
研究人员功能地表达了人类α6β4尼古丁乙胆受体 (nAChR),并通过激动剂确定了其冷-EM结构. 这推动了针对这一重要的nAChR亚型的治疗疼痛的药物发现.
科学领域:
- 神经科学和药理学 神经科学和药理学
- 结构生物学 结构生物学
- 药物发现 药物发现 药物发现
背景情况:
- 阿尔法6β4尼古丁性乙胆受体 (nAChR) 是治疗疼痛的关键治疗标.
- 阿尔法6β4 nAChR的功能表达一直是一个重大挑战,限制了药物开发.
- 了解alpha6beta4 nAChR的结构和配体相互作用对于开发向疗法至关重要.
研究的目的:
- 为了实现人类alpha6beta4的功能表达,nAChR.
- 为了确定alpha6beta4 nAChR与激动剂复合的冷电子显微镜 (cryo-EM) 结构.
- 阐明对alpha6beta4 nAChR的联结和亲缘关系的分子基础.
主要方法:
- 在合适的系统中,人类alpha6beta4 nAChR的功能表达.
- 低温电子显微镜 (cryo-EM) 用于解析高分辨率结构.
- 生物化学和结构分析以确定连接物结合点和关键残留物.
主要成果:
- 成功实现了人类alpha6beta4nAChR的功能表达.
- 确定alpha6beta4 nAChR与尼古丁和特巴尼克林复合的冷-EM结构,在无敏状态下.
- 确定了受体作为2α6:3β4子单元的固态度,并确定了特定的结合口袋和对激素相互作用至关重要的残留物.
结论:
- 这项研究为人类alpha6beta4 nAChR.提供了第一个功能表达和结构洞察力.
- 详细了解agonist与alpha6beta4 nAChR的结合的详细分子理解,解释不同的亲和力.
- 这些发现为合理的药物设计铺平了道路,针对α6β4 nAChR缓解疼痛.
相关概念视频
Cholinergic Receptors: Nicotinic
2.0K
Nicotinic receptors are ligand-gated ion channels that are activated by acetylcholine and nicotine. Upon activation, they cause a rapid increase in the permeability of cells to K+, Na+, and Ca2+, followed by depolarization and excitation. They are in the autonomic ganglia, skeletal neuromuscular junction, CNS, and adrenal medulla.
There are two types of nicotinic receptors: neuromuscular (NM/NM/N1) and neuronal (NN/NN/N2). The two families differ based on their location and selectivity to...
There are two types of nicotinic receptors: neuromuscular (NM/NM/N1) and neuronal (NN/NN/N2). The two families differ based on their location and selectivity to...
2.0K
Ligand-Gated Ion Channel Receptor: Gating Mechanism
2.0K
Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...
2.0K
Cholinergic Receptors: Muscarinic
1.6K
The pharmacological actions of acetylcholine are elicited via its binding to two families of cholinergic receptors or cholinoceptors, namely, muscarinic and nicotinic receptors. Muscarinic receptors are G protein-coupled receptors and have five subtypes, M1–M5. All mAChR subtypes are activated by acetylcholine and blocked by the antagonist, atropine.
The subtypes M1, M3, and M5 couple with the Gq subunit and activate the phospholipase C (PLC) activity, mobilizing intracellular Ca2+....
The subtypes M1, M3, and M5 couple with the Gq subunit and activate the phospholipase C (PLC) activity, mobilizing intracellular Ca2+....
1.6K
Ligand-gated Ion Channels
12.0K
Ligand-gated ion channels are transmembrane proteins with a channel for ions to pass through and a binding site for a ligand. The channel opens only when a ligand attaches to the binding site.
Three Subfamilies of Ligand-gated Ion Channels
Ligand-gated ion channels fall into three subfamilies. The 'Cys-loop' includes the nicotinic acetylcholine receptors, γ-aminobutyric acid (GABA), glycine, and 5-hydroxytryptamine receptors. The second one is the 'Pore-loop' channels that...
Three Subfamilies of Ligand-gated Ion Channels
Ligand-gated ion channels fall into three subfamilies. The 'Cys-loop' includes the nicotinic acetylcholine receptors, γ-aminobutyric acid (GABA), glycine, and 5-hydroxytryptamine receptors. The second one is the 'Pore-loop' channels that...
12.0K
Direct-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
801
Cholinergic agonists or cholinomimetics mimic the action of acetylcholine to stimulate the parasympathetic nervous system. They are categorized into direct-acting and indirect-acting agents. The direct-acting cholinergic drugs induce the parasympathetic response by directly binding to the muscarinic or nicotine receptors. In comparison, the indirect-acting cholinergic drugs prevent acetylcholine hydrolysis, indirectly contributing to the extended parasympathetic response.
The direct-acting...
The direct-acting...
801
Cholinergic Antagonists: Chemistry and Structure-Activity Relationship
2.0K
Cholinergic antagonists bind to cholinergic receptors and limit the effects of acetylcholine and other cholinergic agonists. Based on the specific cholinergic receptor affinity, these antagonists are classified as muscarinic or nicotinic. Anticholinergics interrupt parasympathetic innervations while sympathetic innervations remain uninterrupted. Muscarinic antagonists are also called 'muscarinic antagonists', 'antimuscarinics', or 'parasympatholytics'. Nicotinic...
2.0K


