新出现的调节神经调节G蛋白合受体的调节方式
Alberto J Gonzalez-Hernandez1, Hermany Munguba2, Joshua Levitz2
1Department of Biochemistry, Weill Cornell Medicine, New York, NY 10065, USA.
Trends in neurosciences
|June 11, 2024
概括
最近的进展揭示了神经系统中G蛋白合受体 (GPCRs) 的新型调节. 了解这些神经调节GPCR机制是治疗神经系统疾病的关键.
科学领域:
- 神经科学是一个神经科学.
- 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:
- G蛋白结合受体 (GPCRs) 是神经元功能的关键调节者,影响刺激性,突触传输和行为.
- 尽管它们很重要,但在特定的神经生理学环境中调整GPCR信号的精确调节机制仍然不完全理解.
- 对神经调节性GPCRs的详细机制理解对于破译它们的生物学作用和开发神经和精神疾病治疗方法至关重要.
研究的目的:
- 审查最近在识别神经调节性GPCRs的新型调节机制方面的进展.
- 为突出管理神经系统GPCR调的新兴原则.
- 在多个生物层面确定未来研究的关键问题.
主要方法:
- 最近科学出版物的文献综述.
- 综合关于GPCR调节的发现,包括G蛋白和受体向机制.
- 分析受体-受体交叉声和突触上下文特定特征.
主要成果:
- 确定神经调节性GPCR调节的新模式.
- 突出显示G蛋白和受体向机制.
- 讨论受体-受体交叉声和独特的突触特征.
结论:
- 新兴的GPCR调原理为其功能提供了新的见解.
- 未来的研究应该解决分子,细胞,突触和神经电路水平.
- 进一步的理解对于神经和精神疾病的治疗应用至关重要.
相关概念视频
G Protein-coupled Receptors
11.8K
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...
11.8K
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
118.2K
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.
118.2K
Activation and Inactivation of G Proteins
7.0K
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...
7.0K
GPCRs Regulate Adenylyl Cylase Activity
5.5K
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...
5.5K
GPCR Desensitization
6.0K
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...
6.0K


