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Activation and Inactivation of G Proteins01:22

Activation and Inactivation of G Proteins

6.5K
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...
6.5K
GPCR Desensitization01:12

GPCR Desensitization

5.6K
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...
5.6K
G-protein Coupled Receptors01:21

G-protein Coupled Receptors

112.8K
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.
112.8K
GPCRs Regulate Adenylyl Cylase Activity01:09

GPCRs Regulate Adenylyl Cylase Activity

5.1K
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...
5.1K
Amplifying Signals via Enzymatic Cascade01:22

Amplifying Signals via Enzymatic Cascade

8.2K
When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
8.2K
G-Protein Gated Ion Channels01:21

G-Protein Gated Ion Channels

4.5K
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...
4.5K

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相关实验视频

Updated: May 13, 2025

Parallel Interrogation of β-Arrestin2 Recruitment for Ligand Screening on a GPCR-Wide Scale using PRESTO-Tango Assay
09:03

Parallel Interrogation of β-Arrestin2 Recruitment for Ligand Screening on a GPCR-Wide Scale using PRESTO-Tango Assay

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β-阿雷斯凝结剂调节G蛋白结合受体功能

Preston J Anderson, Peng Xiao, Yani Zhong

    bioRxiv : the preprint server for biology
    |April 16, 2025
    PubMed
    概括

    β-arrestins (β-arrestins) 形成类似液体的冷凝物,调节G蛋白结合受体 (GPCR) 信号传递. 这一过程由靠近GPCRs的β-arrestin寡合化驱动,将信号分隔并控制受体功能.

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    Monitoring GPCR-β-arrestin1/2 Interactions in Real Time Living Systems to Accelerate Drug Discovery
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    相关实验视频

    Last Updated: May 13, 2025

    Parallel Interrogation of β-Arrestin2 Recruitment for Ligand Screening on a GPCR-Wide Scale using PRESTO-Tango Assay
    09:03

    Parallel Interrogation of β-Arrestin2 Recruitment for Ligand Screening on a GPCR-Wide Scale using PRESTO-Tango Assay

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    Monitoring GPCR-β-arrestin1/2 Interactions in Real Time Living Systems to Accelerate Drug Discovery
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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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    科学领域:

    • 蜂信号传输是如何进行的
    • 分子生物学分子生物学
    • 结构生物学是结构生物学.

    背景情况:

    • G蛋白结合受体 (GPCRs) 对细胞功能至关重要,是最大的受体家族.
    • β-arrestins (β-arrestins) 是GPCR信号传递的关键调节者,调解脱敏,内化和各种信号通路.
    • 通过β-阿雷斯调节各种GPCR功能的精确机制仍然不完全理解.

    研究的目的:

    • 调查β-arrestin寡合化和液液相分离 (LLPS) 在GPCR调控中的作用.
    • 阐明β-结凝聚物如何影响GPCR内部化和信号动态.

    主要方法:

    • 使用冷电子显微镜 (cryo-EM) 来确定GPCR-β-arrestin复合物的结构.
    • 研究了靠近GPCRs的β-arrestin寡合化.
    • 分析了β-arrestin凝结物的形成及其对GPCR功能的影响.

    主要成果:

    • 证明β-arrestins经历液-液相分离 (LLPS) 形成功能凝结物.
    • 表明,由GPCR复合体内的特定方向促进的β-arrestin寡合化对于凝结物形成至关重要.
    • 观察到,这些β-结凝聚物调节GPCR内部化和信号传递.

    结论:

    • 通过LLPS形成的β-arrestin凝聚物代表了调节GPCR功能的新范式.
    • β-阿雷斯的LLPS促进了受体水平的信号分隔.
    • 对GPCR-β-arrestin复合体的结构洞察力为β-arrestin介导调节提供了机制基础.