活性β-arrestin-1结合G蛋白结合受体的结构
Arun K Shukla1, Aashish Manglik, Andrew C Kruse
1Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.
Nature
|April 23, 2013
概括
研究人员揭示了活性β-arrestin-1 (arrestin-2) 与酸化V2压缩素受体结合的高分辨率结构. 这种结构阐明了β-逮捕因子激活机制和G蛋白结合受体 (GPCR) 信号传递的受体相互作用.
科学领域:
- 分子生物学分子生物学
- 结构生物学 结构生物学
- 生物化学 生物化学
背景情况:
- G-蛋白合受体 (GPCRs) 是由G蛋白,GRKs和逮捕蛋白进行调节的.
- 阻断中介受体脱敏化和G蛋白独立信号传递.
- 阿雷斯激活和GPCR相互作用的结构基础尚不清楚.
研究的目的:
- 为了阐明β-arrestin激活的结构机制.
- 了解激活β-arrestin和GPCRs之间的相互作用.
主要方法:
- 结晶结构确定与酸化V2压缩素受体 (V2Rpp) 复合的β-arrestin-1.
- 利用一种形状选择性抗体片段 (Fab30) 来稳定β-arrestin-1.0的活性状态.
主要成果:
- 揭示了β-arrestin-1-V2Rpp-Fab30复合物的高分辨率晶体结构.
- 在β-arrestin-1中观察到显著的构造变化,包括域旋转和拉里亚特循环重定位.
- 在激活的β-arrestin-1.1上确定了一个独特的受体相互作用接口.
结论:
- 这项研究提供了详细的结构理解的β-arrestin激活.
- 这些发现表明,β-止素激活和GPCR相互作用的一般分子机制.
- 这项工作为了解阿里斯在GPCR信号和调节中的作用奠定了基础.
相关概念视频
Assembly of Signaling Complexes
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,...
Activation and Inactivation of G Proteins
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 affinity and are together...
G-protein Coupled Receptors
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.
G-protein Coupled Receptors
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.
Amplifying Signals via Enzymatic Cascade
When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze the...
GPCR Desensitization
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...


