了解一些B1类GPCR家族成员的结构和激活机制
Hayrunisa Aksu1, Ayşenur Demirbilek1, Abdullahi Ibrahim Uba2
1Department of Molecular Biology and Genetics, Istanbul AREL University, Istanbul, 34537, Turkey.
Molecular biology reports
|September 6, 2024
概括
B1类GPCRs对于糖尿病治疗至关重要,通过涉及细胞外和膜外域的两步机制激活. 结构洞察力揭示了激素受体相互作用驱动细胞反应.
科学领域:
- 生物化学 生物化学
- 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:
- B1类GPCR是具有大型N终端细胞外域 (ECD) 的多类激素受体.
- 这些受体,包括GIPR,GCGR,GLP1R和GLP2R,都与糖尿病的发病有关.
- 了解它们的激活对于开发糖尿病疗法至关重要.
研究的目的:
- 审查B1类GPCR及其激活机制的结构细节.
- 为了突出显示受体激活后的形状变化.
- 讨论分子动力学 (MD) 模拟在表征这些变化的作用.
主要方法:
- 实验结构数据的分析 (X射线晶体学,冷EM,NMR).
- 对B1类GPCR激活现有文献的审查.
- 简要讨论MD模拟应用程序.
主要成果:
- 乙1类GPCR激活遵循涉及ECD和跨膜 (TM) 域相互作用的两步模型.
- 激素C-终端与ECD结合,而N-终端与TM域相互作用,传输信号.
- 结构数据显示了激活过程中的关键形状变化.
结论:
- 结构研究正在揭开B1类GPCRs的激活机制.
- 这种知识有助于理解受体功能和设计新型连接体.
- 进一步的结构探索和MD模拟可以指导糖尿病的未来药物设计.
相关概念视频
Transducer Mechanism: G Protein–Coupled Receptors
1.9K
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,...
GPCRs are also called heptahelical,...
1.9K
G Protein-coupled Receptors
11.6K
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...
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...
11.6K
Activation and Inactivation of G Proteins
6.9K
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...
6.9K
GPCRs Regulate Adenylyl Cylase Activity
5.4K
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...
5.4K
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...
Sensory...
4.5K
GPCR Desensitization
5.9K
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...
5.9K


