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无去污剂的配体结合家族 B G 蛋白偶联受体的基于聚合物的无细胞表达。

Polymer-based cell-free expression of ligand-binding family B G-protein coupled receptors without detergents.

机构信息

Structural Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.

出版信息

Protein Sci. 2011 Jun;20(6):1030-41. doi: 10.1002/pro.636. Epub 2011 May 3.

Abstract

G-protein coupled receptors (GPCRs) constitute the largest family of intercellular signaling molecules and are estimated to be the target of more than 50% of all modern drugs. As with most integral membrane proteins (IMPs), a major bottleneck in the structural and biochemical analysis of GPCRs is their expression by conventional expression systems. Cell-free (CF) expression provides a relatively new and powerful tool for obtaining preparative amounts of IMPs. However, in the case of GPCRs, insufficient homogeneity of the targeted protein is a problem as the in vitro expression is mainly done with detergents, in which aggregation and solubilization difficulties, as well as problems with proper folding of hydrophilic domains, are common. Here, we report that using CF expression with the help of a fructose-based polymer, NV10 polymer (NVoy), we obtained preparative amounts of homogeneous GPCRs from the three GPCR families. We demonstrate that two GPCR B family members, corticotrophin-releasing factor receptors 1 and 2β are not only solubilized in NVoy but also have functional ligand-binding characteristics with different agonists and antagonists in a detergent-free environment as well. Our findings open new possibilities for functional and structural studies of GPCRs and IMPs in general.

摘要

G 蛋白偶联受体 (GPCRs) 构成了细胞间信号分子的最大家族,据估计,它们是超过 50%的现代药物的靶点。与大多数整合膜蛋白 (IMPs) 一样,GPCRs 的结构和生化分析的主要瓶颈是它们在常规表达系统中的表达。无细胞 (CF) 表达为获得大量 IMP 提供了一种相对较新且强大的工具。然而,就 GPCR 而言,目标蛋白的均一性不足是一个问题,因为体外表达主要使用去污剂进行,其中常见的问题是聚集和溶解困难,以及亲水区正确折叠的问题。在这里,我们报告说,使用基于果糖的聚合物 NV10 聚合物 (NVoy) 进行 CF 表达,我们从三个 GPCR 家族中获得了大量均一的 GPCR。我们证明,两种 GPCR B 家族成员,促肾上腺皮质释放因子受体 1 和 2β不仅在 NVoy 中可溶解,而且在无去污剂环境中,它们还具有与不同激动剂和拮抗剂结合的功能性配体结合特性。我们的发现为 GPCR 和一般 IMP 的功能和结构研究开辟了新的可能性。

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