人类大麻素受体CB2-Gi信号综合体的冷EM结构
Changrui Xing1, Youwen Zhuang2, Ting-Hai Xu3
1Department of Pharmaceutical Sciences, Computational Chemical Genomics Screen Center, School of Pharmacy, and NIDA National Center of Excellence for Computational Drug Abuse Research, University of Pittsburgh, Pittsburgh, PA 15261, USA; Drug Discovery Institute and Departments of Computational Biology and of Structural Biology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
研究人员发现了CB2受体信号复合体的结构,揭示了WIN 55,212-2等激动剂如何结合. 这一发现有助于设计出无CB1副作用的治疗疼痛和炎症的新药.
科学领域:
- 结构生物学
- 神经药理学
- 生物化学
背景情况:
- 大麻素受体2 (CB2) 药物为神经退行性疾病,炎症和疼痛提供治疗潜力.
- 选择性CB2药物避免与CB1受体激活相关的心理副作用.
- 了解CB2激活和信号机制对于有效的药物开发至关重要.
研究的目的:
- 阐明CB2受体激活和G蛋白合的结构基础.
- 确定区分CB2激动剂和抗剂的结构决定因素.
- 为基于结构的药物设计提供CB2受体功能的见解.
主要方法:
- 电子显微镜 (cryo-EM) 来确定人类CB2-Gi信号复合物的结构.
- 与激动剂WIN 55,212-2进行联合结晶.
- 计算对接和新型激励剂和对抗剂的合理设计.
主要成果:
- 确定了与WIN 55,212-2结合的人类CB2-Gi复合物的冷-EM结构.
- 确定了控制连体结合和受体激活的关键结构特征.
- 在受体激活,配体识别和Gi合方面发现了CB2和CB1之间的显著差异.
结论:
- 确定的结构提供了对CB2受体信号的分子理解.
- 结构洞察力有助于选择性CB2激动剂和抗剂的合理设计.
- 这项研究为开发针对大麻素系统的新疗法铺平了道路.
更多相关视频
09:09Preparation and Delivery of Protein Microcrystals in Lipidic Cubic Phase for Serial Femtosecond Crystallography
Published on: September 20, 2016
14:02Optimizing the Genetic Incorporation of Chemical Probes into GPCRs for Photo-crosslinking Mapping and Bioorthogonal Chemistry in Live Mammalian Cells
Published on: April 9, 2018
相关概念视频
G Protein-coupled Receptors
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...
Assembly of Signaling Complexes
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
Transducer Mechanism: G Protein–Coupled Receptors
GPCRs are also called heptahelical,...
G-protein Coupled Receptors
GPCR Desensitization
IP3/DAG Signaling Pathway
