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相关概念视频

G-Protein Gated Ion Channels01:21

G-Protein Gated Ion Channels

5.6K
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...
5.6K
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 Receptors01:15

G Protein-coupled Receptors

16.5K
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...
16.5K
GPCRs Regulate Adenylyl Cylase Activity01:09

GPCRs Regulate Adenylyl Cylase Activity

7.3K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
7.3K
IP3/DAG Signaling Pathway01:11

IP3/DAG Signaling Pathway

14.2K
Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and...
14.2K
GPCR Desensitization01:12

GPCR Desensitization

7.9K
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...
7.9K

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相关实验视频

Updated: Jan 13, 2026

Construction of Model Lipid Membranes Incorporating G-protein Coupled Receptors GPCRs
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Construction of Model Lipid Membranes Incorporating G-protein Coupled Receptors GPCRs

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人类B1类GPCR通过血脂的调节.

Kin W Chao1,2,3, Linda Wong4, Affiong I Oqua4

  • 1Department of Life Sciences, Sir Ernst Chain Building, Imperial College London, London, UK.

Communications biology
|January 8, 2026
PubMed
概括
此摘要是机器生成的。

B1类G蛋白结合受体 (GPCRs) 与胆固醇和PIP2等脂质以状态依赖的方式相互作用. 这些脂质相互作用在整个亚家族中得到保存,并影响受体动态,影响药物发现.

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Author Spotlight: Developing Parmodulins to Target Protease-Activated Receptors for Inflammation Control
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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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相关实验视频

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Construction of Model Lipid Membranes Incorporating G-protein Coupled Receptors GPCRs
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Author Spotlight: Developing Parmodulins to Target Protease-Activated Receptors for Inflammation Control
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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:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 药理学 药理学是指药理学的学科.

背景情况:

  • B1类G蛋白结合受体 (GPCRs) 对新陈代谢,神经元活动和药物开发至关重要.
  • 脂质显著调节GPCR信号传递,但与B1类GPCRs的详细分子相互作用尚不清楚.

研究的目的:

  • 在活性和非活性状态下研究脂质和15个人类B1类GPCR之间的分子级相互作用.
  • 在B1类GPCR亚家族中识别脂质受体相互作用的保存模式.

主要方法:

  • 15个人类B1类GPCR的粗粒度分子动力学 (MD) 模拟.
  • 在复杂的等离子膜中利用aiida-gromacs进行模拟设置.
  • 在体外进行时间解析的弗斯特尔共振能量转移 (FRET) 试验.

主要成果:

  • B1类GPCRs在特定的表面位置与胆固醇和酸氨酸-4,5-双酸盐 (PIP2) 呈现状态依赖的相互作用.
  • 在GPCR亚系中发现了脂质相互作用动态的保存模式.
  • 发现甘氨基脂GM3调节了B1类细胞外域的动态.

结论:

  • 脂质相互作用是B1类GPCRs功能状态的组成部分.
  • 了解这些保存的脂质-GPCR动态,可以为开发向治疗提供信息.
  • GM3在调节B1类GPCR细胞外域动态方面发挥着重要作用.