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Updated: Jul 29, 2026

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Measuring G-protein-coupled Receptor Signaling via Radio-labeled GTP Binding
Published on: June 9, 2017
人体血管压素V2受体的溶液NMR光谱,一种G蛋白结合受体
Changlin Tian1, Richard M Breyer, Hak Jun Kim
1Center for Structural Biology and Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-8725, USA.
Journal of the American Chemical Society
|June 2, 2005
概括
获得了人类血管压素V2受体的高质量的NMR光谱,这是一个关键的G蛋白结合受体 (GPCR). 这一突破使GPCRs的详细结构研究成为可能,这对于了解健康和疾病至关重要.
科学领域:
- 生物化学 生物化学
- 结构生物学 结构生物学
- 药理学 药理学是指药理学的学科.
背景情况:
- G蛋白结合受体 (GPCR) 是关键的膜蛋白,参与许多生理过程.
- GPCRs的功能障碍与各种人类疾病有关,使它们成为重要的药物标.
- 了解GPCR结构对于合理的药物设计和治疗开发至关重要.
研究的目的:
- 为人类GPCR,压素V2受体呈现精确的解决方案核磁共振 (NMR) 光谱.
- 为了证明脊柱共振分配对大多数受体共振的可行性.
- 建立一种可靠的方法,从膜结合的GPCR中获取高质量的NMR数据.
主要方法:
- 血管压素V2受体在膜中的表达,避免包含体的形成.
- 提取和净化受体使用生物化学上温和的脂清洁剂.
- 在洗剂小粒中准备NMR样本,用于溶液NMR光谱学.
主要成果:
- 获得了人类血管压素V2受体的良好分辨率溶液NMR光谱.
- 证明了对于大多数共振来说,骨干共振分配是可行的.
- 确定了表达,提取和洗剂方法的特定组合,这对于高质量的光谱至关重要.
结论:
- 提出的方法允许使用NMR进行高分辨率的GPCR结构研究.
- 这项工作为未来对GPCR结构功能关系的研究提供了基础.
- 这些发现对于针对GPCRs的药物发现具有重要意义.
相关概念视频
G-protein Coupled Receptors
G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
G Protein-coupled Receptors
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...
Activation and Inactivation of G Proteins
Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high affinity and are together...
GPCR Desensitization
G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...
Transducer Mechanism: G Protein–Coupled Receptors
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to various stimuli. GPCRs regulate critical physiological pathways and are excellent drug targets for treating diseases such as diabetes, cancer, obesity, depression, or Alzheimer's. Nearly 35% of approved drugs implement their therapeutic effects by selectively interacting with specific GPCRs.
GPCRs are also called heptahelical, 7TM, or...
GPCRs are also called heptahelical, 7TM, or...
Transducer Mechanism: Enzyme-Linked Receptors
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:

