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Cooperative Allosteric Transitions01:58

Cooperative Allosteric Transitions

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Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...
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Allosteric Regulation01:08

Allosteric Regulation

57.6K
Allosteric regulation of enzymes occurs when the binding of an effector molecule to a site that is different from the active site causes a change in the enzymatic activity. This alternate site is called an allosteric site, and an enzyme can contain more than one of these sites. Allosteric regulation can either be positive or negative, resulting in an increase or decrease in enzyme activity. Most enzymes that display allosteric regulation are metabolic enzymes involved in the degradation or...
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Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

1.8K
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,...
1.8K
G Protein-coupled Receptors01:15

G Protein-coupled Receptors

11.2K
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...
11.2K
GPCRs Regulate Adenylyl Cylase Activity01:09

GPCRs Regulate Adenylyl Cylase Activity

5.2K
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...
5.2K
GPCR Desensitization01:12

GPCR Desensitization

5.8K
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...
5.8K

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Updated: Jun 2, 2025

Visualizing the Conformational Dynamics of Membrane Receptors Using Single-Molecule FRET
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Visualizing the Conformational Dynamics of Membrane Receptors Using Single-Molecule FRET

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在C类GPCR阳性基调节中的合规多样性.

Giuseppe Cannone1, Ludovic Berto2, Fanny Malhaire2

  • 1MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.

Nature communications
|January 13, 2025
PubMed
概括

阳性全调节剂 (PAMs) 通过结合到不同的位点来改变元类谷氨酸受体5 (mGlu5) 的功能,从而影响受体平衡和形状变化. 这揭示了PAMs如何调节mGlu5受体活性,用于潜在的治疗应用.

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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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G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay
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相关实验视频

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Visualizing the Conformational Dynamics of Membrane Receptors Using Single-Molecule FRET
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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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G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay
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科学领域:

  • 神经科学是一个神经科学.
  • 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:

  • 甲基酸盐受体 (mGluRs) 是C类G蛋白合受体,对神经传递至关重要.
  • 像mGlu5一样,mGluRs由L-氨酸激活,并且具有与跨膜域 (7TM) 连接的金星飞 (VFT) 域.
  • 阳性基调节剂 (PAM) 向7TM域,以增强mGluR信号传递,为神经系统疾病提供治疗潜力.

研究的目的:

  • 阐明不同的PAMs调节元托基质谷氨酸受体5 (mGlu5) 的结构机制.
  • 了解PAM结合如何影响mGlu5受体的结构格局和功能状态.
  • 识别中间受体状态及其相关相互作用.

主要方法:

  • 使用冷电子显微镜 (cryo-EM) 来确定mGlu5受体复合物的结构.
  • 用三种化学和药理学上不同的PAMs净化mGlu5受体.
  • 结构分析的重点是PAM结合模式及其对受体构成的影响.

主要成果:

  • 化EM结构揭示了mGlu5受体上三种不同的PAM的独特结合模式.
  • 发现PAMs调节受体平衡,通过它们在7TM域内的相互作用将其转移到活性状态.
  • 确定了无PAM,激动剂结合的中间状态,突出显示了涉及细胞内循环2的相互作用.

结论:

  • PAMs通过与7TM域结合来全质调节mGlu5受体活性,从而影响其构造平衡.
  • PAMs的独特结合方式解释了它们对mGlu5受体功能的多种影响.
  • 了解这些结构和功能关系是开发针对神经疾病的向治疗方法的关键.