GPCRs与受体活性修饰蛋白的相互作用组的多重映射
Ilana B Kotliar1,2, Annika Bendes3, Leo Dahl3
1Laboratory of Chemical Biology and Signal Transduction, The Rockefeller University, New York, NY, USA.
Science advances
|July 31, 2024
概括
受体活性修饰蛋白 (RAMPs) 与许多G蛋白结合受体 (GPCRs) 相互作用,影响其功能. 这项研究绘制了这些GPCR-RAMP相互作用的地图,确定了新的治疗点.
科学领域:
- 生物化学 生物化学
- 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:
- 受体活性修饰蛋白 (RAMPs) 调节G蛋白结合受体 (GPCR) 贩运和药理学.
- 之前的研究发现了RAMP与大约50个GPCR的相互作用,但详细表征仍然有限.
研究的目的:
- 为了全面地绘制GPCR-RAMP互动组.
- 为潜在的治疗向确定新的GPCR-RAMP复合体.
主要方法:
- 创建了一个215个双位标记 (DuET) GPCRs的库,涵盖所有子家族.
- 每个GPCR与三个RAMP中的每一个共同表达.
- 使用多重悬浮珠子阵列 (SBA) 免疫试验在三个细胞系中选的相互作用.
主要成果:
- 确定了122个GPCRs,有证据表明它们与至少一个RAMP相互作用.
- 发现了23种内源表达的GPCRs,与RAMPs形成复合体.
- 建立了一个全面的GPCR-RAMP互动原子图.
结论:
- 这项研究显著扩大了RAMP相互作用的GPCRs已知的功能特征.
- 已识别的GPCR-RAMP复合体代表了开发选择性治疗的潜在目标.
- 这种相互作用组映射为未来药物发现努力提供了基础,目标是针对GPCR-RAMP信号通路.
相关概念视频
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
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
Assembly of Signaling Complexes
5.7K
Multiprotein signaling complexes are formed in a dynamic process involving protein-protein interactions at the cytoplasmic domain of transmembrane receptors or enzymatic and non-enzymatic proteins associated with the receptor. These complexes ensure the activation and propagation of intracellular signals that regulate cell functions.
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
5.7K
G-protein Coupled Receptors
117.5K
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.
117.5K
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
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


