GPCR激活的一个非正规机制
Alexander S Powers1,2,3,4,5, Aasma Khan6, Joseph M Paggi2,3,4,5
1Department of Chemistry, Stanford University, Stanford, CA 94305, USA.
bioRxiv : the preprint server for biology
|August 30, 2023
概括
某些药物分子通过重新安排细胞内循环来激活G蛋白合受体 (GPCR),而不仅仅是跨膜螺旋. 这一发现为开发精确的GPCR向药物提供了新的策略.
科学领域:
- 生物化学 生物化学
- 药理学 药理学是指药理学的学科.
- 分子生物学分子生物学
背景情况:
- G蛋白结合受体 (GPCR) 是关键的药物标,它们的信号机制得到了广泛的研究.
- 目前的理解认为,GPCR激动剂通过跨膜螺旋体重组激活受体.
- 精确控制GPCR信号传输是开发更安全,更有效的治疗方法的关键.
研究的目的:
- 为了研究GPCR激活的替代分子机制,超出跨膜螺旋体重排.
- 探索用于精确控制GPCR信号传递的新策略.
主要方法:
- 原子层次的模拟以建模配体-受体相互作用.
- 针对性的突变发生,以验证模拟预测.
- 生物化学测试以评估受体激活和传感器蛋白质结合.
主要成果:
- 证明特定的激动剂通过直接重新安排细胞内循环来激活自由脂肪酸受体1.
- 通过突变发生过程验证模拟结果,通过破坏循环相互作用将激动剂转化为逆激动剂.
- 确定了一种用于GPCR调节的新型全性机制.
结论:
- GPCR激活可以通过细胞内循环重组进行调解,从而挑战现有的模型.
- 这种机制为代性联结体设计提供了新的途径,针对许多GPCR.
- 开发具有高度特异性的药物,改善治疗结果的潜力.
相关概念视频
GPCRs Regulate Adenylyl Cylase Activity
5.7K
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...
5.7K
Activation and Inactivation of G Proteins
7.2K
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...
7.2K
GPCR Desensitization
6.1K
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...
6.1K
Transducer Mechanism: G Protein–Coupled Receptors
2.1K
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,...
2.1K
G Protein-coupled Receptors
12.2K
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...
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...
12.2K
G-protein Coupled Receptors
120.2K
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.
120.2K


