全长型B类葡萄糖蛋白结合受体的结构
Haonan Zhang1,2, Anna Qiao1,2, Dehua Yang1,3
1CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Pudong, Shanghai 201203, China.
Nature
|May 18, 2017
概括
全长的人类葡萄糖受体 (GCGR) 晶体结构显示其无活性构造. 关键的结构元素,包括茎和细胞外环,对GCGR至关重要
科学领域:
- 结构生物学
- 生物化学
- 内分泌学
背景情况:
- 人类葡萄糖受体 (GCGR) 是B类G蛋白合受体,对葡萄糖平衡至关重要.
- GCGR与2型糖尿病的病理生理学有关.
- 之前的结构研究集中在GCGR跨膜领域.
研究的目的:
- 为了确定全长人体GCGR的晶体结构.
- 阐明树干和细胞外环在 GCGR 功能中的结构作用.
主要方法:
- 射线晶体学 (3.0 Å 分辨率)
- -交换
- 双硫化物交叉连接
- 分子动力学模拟
主要成果:
- 在非活性状态下解决了全长GCGR的晶体结构.
- 茎区域采用β-链形状,连接细胞外和膜外域.
- 第一个细胞外环形成β毛针,与茎相互作用形成β片.
- 茎和第一个细胞外环对于调节连接体结合和受体激活至关重要.
结论:
- 全长度的GCGR结构为非活性受体构造提供了新的见解.
- 茎和第一个细胞外环在GCGR信号传递中起着重要作用.
- 了解这些结构特征可以更深入地了解B类GPCR机制.
相关概念视频
Transducer Mechanism: G Protein–Coupled Receptors
5.7K
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,...
5.7K
G Protein-coupled Receptors
18.3K
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...
18.3K
G-protein Coupled Receptors
133.1K
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.
133.1K
Activation and Inactivation of G Proteins
11.9K
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...
11.9K
GPCRs Regulate Adenylyl Cylase Activity
7.8K
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...
7.8K
GPCR Desensitization
8.4K
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...
8.4K


