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相关概念视频

G Protein-coupled Receptors01:15

G Protein-coupled Receptors

16.3K
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...
16.3K
Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

3.9K
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,...
3.9K
G-protein Coupled Receptors01:21

G-protein Coupled Receptors

131.3K
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.
131.3K
G-Protein Gated Ion Channels01:21

G-Protein Gated Ion Channels

5.5K
GPCRs are primarily responsible for our sense of smell, taste, and vision.  The binding of a sensory stimulus activates GPCR to stimulate effector proteins, many of which are ion channels in the sensory organs. GPCRs modulate the opening and closing of the target ion channels either directly by binding them, or by releasing second messengers that activate these channels. As ions move across the membrane, the membrane potential is altered, which induces an appropriate response.
Sensory...
5.5K
GPCR Desensitization01:12

GPCR Desensitization

7.8K
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...
7.8K
Activation and Inactivation of G Proteins01:22

Activation and Inactivation of G Proteins

10.7K
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...
10.7K

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Measuring G-protein-coupled Receptor Signaling via Radio-labeled GTP Binding
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Measuring G-protein-coupled Receptor Signaling via Radio-labeled GTP Binding

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简要的药理学指南 2025/26:G蛋白结合受体

Stephen P H Alexander1, Anthony P Davenport2, Eamonn Kelly3

  • 1Division of Physiology, Pharmacology & Neuroscience, School of Life Sciences, University of Nottingham Medical School, Nottingham, NG7 2UH, UK.

British journal of pharmacology
|December 29, 2025
PubMed
概括

药理学简要指南2025/26提供了对人类药物点及其相互作用的精心策划的概述. 这本两年一次的出版物提供了基本的药理学数据,并确定了研究的选择性工具.

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A Kinetic Fluorescence-based Ca2+ Mobilization Assay to Identify G Protein-coupled Receptor Agonists, Antagonists, and Allosteric Modulators
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A Kinetic Fluorescence-based Ca2+ Mobilization Assay to Identify G Protein-coupled Receptor Agonists, Antagonists, and Allosteric Modulators
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科学领域:

  • 药理学 药理学是指药理学的学科.
  • 药物发现 药物发现 药物发现
  • 生物医学科学 生物医学科学

背景情况:

  • 英国药理学杂志每两年出版一次的药理学简要指南.
  • 本指南提供了对药物目标家族的比较概述.
  • 它是全面的药理学指南网站的缩写版本.

研究的目的:

  • 提供对人类药物点的清晰,易于理解和结构良好的总结.
  • 为选择性药理工具提供专家策划的建议.
  • 作为药理信息的永久,可引用,及时记录.

主要方法:

  • 大约1900个人类药物点的关键药理性质的总结.
  • 包含了近7000个相互作用,涉及约4400个连接体.
  • 与国际基础和临床药理学联盟 (NC-IUPHAR) 合作,为官方命名体系提供服务.

主要成果:

  • 2025/26年版涵盖了六个主要目标家族:G蛋白合受体,离子通道,核激素受体,催化受体,酶和输送器.
  • 提供了有关命名的信息,简要的摘要,以及最好的可用的药理学工具.
  • 包括关键参考文献和进一步阅读的建议.

结论:

  • "简要指南"是研究人员需要稳定,可引用的参考资料的宝贵资源.
  • 它通过提供药理学数据的永久记录来补充在线数据库.
  • 该指南有助于识别药物点和选择适当的药理工具.