Purification & Structural Analysis/Cannabinoid Receptor

纯化

• 批准号: 7266944
• 负责人: David L Farrens
• 金额: $ 21.48万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-08-15 至 2010-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7266944
• 关键词: Address; Adrenergic Receptor; Affinity; Agonist; Alanine; Binding; Biochemical; Buffers; CNR1 gene; Cannabinoids; Condition; Crystallization; Cysteine; Data; Development; Event; Family; G-Protein-Coupled Receptors; GTP-Binding Proteins; Glaucoma; Goals; Ions; Kinetics; Knowledge; Ligand Binding; Ligand Binding Domain; Ligands; Marijuana; Marijuana Receptor; Measures; Membrane Proteins; Methods; Molecular; Monitor; Mutate; N-terminal; Neurons; Pharmaceutical Preparations; Photoreceptors; Play; Procedures; Process; Property; Proteins; Rate; Receptor Activation; Refractory; Resolution; Retinal; Rhodopsin; Role; Scanning; Staging; Structure; Testing; Therapeutic; Transmembrane Domain; Work; addiction; cannabinoid receptor; chronic pain; comparative; drug of abuse; extracellular; improved; member; receptor; research study; theories

DESCRIPTION (provided by applicant): Marijuana is one of the most widely used drugs of abuse, and is increasingly being ascribed therapeutic properties. Unfortunately, high-resolution structural knowledge about the marijuana receptor, called CB1, is limited. Such knowledge would aid in the development of compounds to better treat addiction, chronic pain and glaucoma. A major obstacle for obtaining CB1 structural information is the fact that CB1 is a membrane protein and thus difficult to obtain in quantities sufficient for traditional structural methods. Furthermore, like most other members of the G-protein coupled receptor family, CB1 is refractory to traditional purification procedures. In Aim I of this CEBRA proposal, we will establish conditions for expressing, solubilizing and purifying large amounts of CB1 to set the stage for crystallization studies. On a parallel track, in Aim II we will express, purify and crystallize two separate CB1 domains, the long CB1 N-terminus, and the transmembrane ligand-binding domain of a truncated form of CBI. Finally, in Aim III we will assess the function, structure and dynamics of extracellular loop E-2 in CBI. The goal of these experiments is to test the emerging hypothesis that this loop plays a universally important role in ligand binding kinetics and receptor stability in GPCRs.

描述（由申请人提供）： 大麻是最广泛使用的滥用药物之一，并且越来越多地被认为具有治疗性质。不幸的是，关于大麻受体CB 1的高分辨率结构知识是有限的。这些知识将有助于开发更好地治疗成瘾、慢性疼痛和青光眼的化合物。 获得CB 1结构信息的一个主要障碍是CB 1是一种膜蛋白，因此难以获得足够数量的传统结构方法。此外，与G蛋白偶联受体家族的大多数其他成员一样，CB 1对传统的纯化方法是难处理的。 在CEBRA提案的目标I中，我们将建立表达、溶解和纯化大量CB 1的条件，为结晶研究奠定基础。在一个平行的轨道上，在目标II中，我们将表达，纯化和结晶两个单独的CB 1结构域，长CB 1 N-末端，和跨膜配体结合结构域的截短形式的CBI。 最后，在目标III中，我们将评估CBI中细胞外环E-2的功能，结构和动力学。这些实验的目的是测试新出现的假设，即该环在GPCR中的配体结合动力学和受体稳定性中起着普遍重要的作用。

项目成果

Monomeric rhodopsin is the minimal functional unit required for arrestin binding.

单体视紫红质是抑制蛋白结合所需的最小功能单元。

• DOI: 10.1016/j.jmb.2010.04.029
• 发表时间: 2010
• 期刊: Journal of molecular biology
• 影响因子: 5.6
• 作者: Tsukamoto,Hisao;Sinha,Abhinav;DeWitt,Mark;Farrens,DavidL
• 通讯作者: Farrens,DavidL

Arrestin can act as a regulator of rhodopsin photochemistry.

Arrestin 可以充当视紫红质光化学的调节剂。

• DOI: 10.1016/j.visres.2006.08.031
• 发表时间: 2006
• 期刊: Vision research
• 影响因子: 1.8
• 作者: Sommer,MarthaE;Farrens,DavidL
• 通讯作者: Farrens,DavidL