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相关概念视频

G-protein Coupled Receptors01:21

G-protein Coupled Receptors

131.6K
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.
131.6K
G Protein-coupled Receptors01:15

G Protein-coupled Receptors

16.6K
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...
16.6K
Quantifying Agonist Activity at G Protein-coupled Receptors11:45

Quantifying Agonist Activity at G Protein-coupled Receptors

19.8K
A method for estimating the affinity constant of an agonist for the active state (Kb) of a G protein-coupled receptor is described. The analysis provides absolute or relative measures of Kb depending on whether constitutive receptor activation is measurable. Our method applies to various responses downstream from receptor...
19.8K
Genetically-encoded Molecular Probes to Study G Protein-coupled Receptors16:16

Genetically-encoded Molecular Probes to Study G Protein-coupled Receptors

15.7K
We genetically-encode the unnatural amino acid, p-azido-L-phenylalanine at various targeted positions in GPCRs and show the versatility of the azido group in different applications. These include a targeted photocrosslinking technology to identify residues in the ligand-binding pocket of a GPCR, and site-specific bioorthogonal modification of GPCRs with a peptide-epitope tag or fluorescent...
15.7K
Construction of Model Lipid Membranes Incorporating G-protein Coupled Receptors (GPCRs)09:45

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

4.0K
This protocol utilizes agarose swelling as a powerful and generalizable technique for incorporating integral membrane proteins (IMPs) into giant unilamellar lipid vesicles (GUVs), as described here for the reconstitution of the human 1A serotonin receptor protein (5-HT1AR), one of the classes of pharmacologically important G protein-coupled...
4.0K
Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

4.0K
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,...
4.0K

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相关实验视频

Updated: Jan 20, 2026

Ligand Binding Receptors : G-protein Coupled Receptors
01:21

Ligand Binding Receptors : G-protein Coupled Receptors

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在G蛋白合受体复合体中信息的传输和处理.

Roger D Jones1, Achille Giacometti2, Alan M Jones3

  • 1Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27514, USA; Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca' Foscari Venezia, 30123 Venezia, Italy; European Centre for Living Technology (ECLT) Ca' Bottacin, 3911 Dorsoduro Calle Crosera, 30123 Venezia, Italy.

Bio Systems
|January 18, 2026
PubMed
概括
此摘要是机器生成的。

我们开发了一种新的热力学模型,用于像G蛋白合受体 (GPCRs) 这样的分子开关. 这个框架揭示了化学流量和能量差异如何控制受体状态,为药物设计提供了洞察力.

关键词:
药物设计 药物设计Entropy EntropyG蛋白结合受体 (GPCR) 是一种诱导适合的形状变化信息流的信息流.没有平衡平衡状态稳定状态.酸酶是一种酸酶.热力学第二定律 热力学第二定律

更多相关视频

Quantifying Agonist Activity at G Protein-coupled Receptors
11:45

Quantifying Agonist Activity at G Protein-coupled Receptors

Published on: December 26, 2011

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G Protein-coupled Receptors
01:15

G Protein-coupled Receptors

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相关实验视频

Last Updated: Jan 20, 2026

Ligand Binding Receptors : G-protein Coupled Receptors
01:21

Ligand Binding Receptors : G-protein Coupled Receptors

131.6K
Quantifying Agonist Activity at G Protein-coupled Receptors
11:45

Quantifying Agonist Activity at G Protein-coupled Receptors

Published on: December 26, 2011

19.8K
G Protein-coupled Receptors
01:15

G Protein-coupled Receptors

16.6K

科学领域:

  • 生物物理学的生物物理.
  • 分子生物学分子生物学
  • 系统生物学 系统生物学

背景情况:

  • G-蛋白合受体 (GPCRs) 对于细胞信号传递至关重要,但它们的切换机制尚未完全理解.
  • 了解GPCR状态转换的物理原理对于破译细胞信息处理至关重要.

研究的目的:

  • 开发生物系统中分子计算的一般理论框架.
  • 将这个框架应用于G蛋白合受体 (GPCRs),以阐明它们的切换机制.
  • 通过非平衡热力学来确定控制GPCR状态转换的关键参数.

主要方法:

  • 开发了一个基于非平衡热力学的理论模型.
  • 确定了受体状态转换的控制参数:化学流量和自由能量差异.
  • 结合了连接体和受体之间的相互形状适应变化.

主要成果:

  • 预测了三个准稳定的GPCR配置:"开启"",关闭"和中间,优化信息传输.
  • 证明活跃状态维持化学流量,而不活跃状态则不.
  • 显示的酸酶活性决定了"开启"/"关闭"状态,而激酶活性保持了流动性.

结论:

  • 该模型为理解由化学流动驱动的生物开关提供了一个可概括的框架.
  • 预测与实验数据一致,表明GPCRs的新药设计目标.
  • 该框架超越了GPCR,扩展到其他生物切换系统.