对人类P2X1受体和连接体相互作用的结构见解
Felix M Bennetts1,2, Hariprasad Venugopal3, Alisa Glukhova2,4
1Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC, Australia.
Nature communications
|September 28, 2024
概括
对P2X1受体的结构洞察力揭示了ATP和NF449的结合方式,指导了未来的药物设计. 这项研究澄清了P2X1受体的功能和调制,用于治疗开发.
科学领域:
- 生物化学和结构生物学
- 药理学 药理学是指药理学的学科.
- 分子医学是分子医学.
背景情况:
- 该P2X1受体,一个三聚体联离子通道,对于泌尿器官和免疫功能至关重要.
- 有限的结构数据和工具化合物阻碍了P2X1受体药物开发.
研究的目的:
- 使用冷EM确定P2X1受体在ATP结合 (无敏化) 和NF449结合 (关闭) 状态中的结构.
- 通过局部导向突变发生来研究P2X1受体激活,抑制和连接体相互作用的分子基础.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于结构阐明.
- 关键残留物参与连接物和金属离子结合的局部定向突变发生.
- 放射性联体结合试验和细胞内离子流入试验,以评估突变效应.
主要成果:
- 在ATP结合无敏化和NF449结合封闭状态下P2X1受体结构的解.
- 与内源性配体ATP相比,对抗剂NF449的明显结合方式.
- 鉴定关键的保存和非保存残留物用于连接体结合和受体调节.
结论:
- 这项研究提供了P2X1受体的高分辨率结构,增强了对其功能的理解.
- 已经确定了控制P2X1受体活性的关键分子相互作用.
- 这些发现为基于结构的in silico药物设计铺平了道路,针对治疗干预措施的P2X1受体.
相关概念视频
Ligand-Gated Ion Channel Receptor: Gating Mechanism
2.2K
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...
2.2K
The Two-State Receptor Model
1.9K
The two-state receptor model explains a drug's interaction with receptors, such as G protein-coupled receptors and ligand-gated ion channels, to induce or inhibit a biological response. When no natural ligands are present, a receptor exists in an equilibrium of inactive (Ri) and active (Ra) conformations. The inactive form does not produce a response, while the active form generates a basal effect known as constitutive activity.
The binding affinity of a drug determines its interaction with...
The binding affinity of a drug determines its interaction with...
1.9K
G Protein-coupled Receptors
11.6K
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
11.6K
Ligand Binding Sites
12.8K
Proteins are dynamic macromolecules that carry out a wide variety of essential processes; however, the activities of most proteins depend on their interactions with other molecules or ions, known as ligands.
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
12.8K
Ligand-gated Ion Channels
12.3K
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...
12.3K
Drug-Receptor Interactions
5.1K
Drug-receptor interaction describes the binding of receptors by drugs, but not all drug-receptor interactions result in activation and tissue response. For instance, the binding of agonists activates the receptor to generate a cellular reaction, while antagonists bind to receptors without causing their activation.
Several parameters, such as the drug's affinity for its receptor and its efficacy, which is its ability to activate the receptor, determine the drug's effect on the tissue....
Several parameters, such as the drug's affinity for its receptor and its efficacy, which is its ability to activate the receptor, determine the drug's effect on the tissue....
5.1K


