INTERHELICAL INTERACTIONS IN THE CANNABINOID RECEPTOR

大麻素受体中的螺旋间相互作用

• 批准号: 6175143
• 负责人: JONATHAN L MCMURRY
• 金额: $ 2.35万
• 依托单位: UNIVERSITY OF CONNECTICUT STORRS
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-06-01 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/6175143
• 关键词: Escherichia coli; G protein; cannabinoid receptor; chimeric proteins; conformation; crosslink; dimer; gel mobility shift assay; membrane proteins; membrane structure; protein structure; protein structure function; receptor coupling; receptor expression; site directed mutagenesis

DESCRIPTION: (Applicant's Abstract) The overall objective of the proposals is to gain structural knowledge of the transmembrane domain of the cannabinoid receptor. Understanding the basis of cannabinoid action as well as design of potential therapeutics requires detailed information about interhelical interactions of transmembrane segments within the protein. The specific aims are to demonstrate the transmembrane segments of the receptor form specific helix-helix interactions, to characterize the nature of those interactions in order to generate structural information, and to reassemble active receptor from fragments to demonstrate the necessity of specific transmembrane segment interactions to receptor function. Transmembrane segments will be expressed as fusion proteins in E. Coli and assayed for their ability to dimerize. Mutations will be designed and made to characterize interactions necessary for dimerization. The data generated will be used to construct a 3-dimensional model of the CB1 transmembrane domain. In order to reassemble active receptor, CB1 will be expressed as pairs of discontinuous fragments that together comprise the full length protein. CB1 reassembly can provide evidence that transmembrane domain of CB1 acts as an organizing center for proper assembly. It is possible that the methods to be employed will be applicable to other membrane proteins, thereby providing the tools necessary to study the structures of other drugs receptors and membrane proteins in general.

描述：（申请人摘要） 这些建议的总体目标是获得以下方面的结构知识： 大麻素受体的跨膜区 了解 大麻素作用的基础以及潜在疗法的设计 需要关于螺旋间相互作用的详细信息， 蛋白质内的跨膜片段。 具体的目的是证明跨膜片段的 受体形式特异性螺旋-螺旋相互作用，以表征 为了产生结构信息， 从片段中重新组装活性受体，以证明 特异性跨膜片段相互作用与受体功能。 跨膜片段在大肠杆菌中表达为融合蛋白。杆菌和 测定它们的二聚化能力。 突变将被设计和制造 以表征二聚化所必需的相互作用。 生成的数据 将用于构建CB 1跨膜的三维模型 域 为了重组活性受体，CB 1将表达为 成对的不连续片段，它们一起构成全长 蛋白 CB 1重组可以提供证据表明， CB 1充当正确装配的组织中心。 所采用的方法可能也适用于其他情况。 膜蛋白，从而提供必要的工具，研究 其他药物受体和一般膜蛋白的结构。