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等离子体波导共振直接监测 G 蛋白偶联受体的组装和配体结合活性。

Direct Monitoring of GPCR Reconstitution and Ligand-Binding Activity by Plasmon Waveguide Resonance.

机构信息

Institute of Chemistry of Membranes and Nanoobjects, UMR 5248 CNRS, University of Bordeaux, Pessac, France.

出版信息

Methods Mol Biol. 2020;2168:123-143. doi: 10.1007/978-1-0716-0724-4_6.

Abstract

The study of G-protein-coupled receptor (GPCR ) mechanisms of activation and signaling often the isolation, purification, and reconstitution of GPCRs in model lipid membranes. GPCR reconstitution from a detergent-micelle system into model membranes is usually a laborious process whose success is tested after the whole process is over by rather indirect methods such as SDS-PAGE and western blotting or by biophysical approaches. Following that, protein activity is measured in yet a different experimental setup. Overall, the whole procedure is tedious, long, and often requires high quantities of material and the use of labeled proteins. Herein, a protocol is described to follow, in a single experimental setup, both GPCR reconstitution from detergent micelles into planar lipid bilayers and its ligand-binding activity using plasmon waveguide resonance. Alternatively, receptor/ligand interactions can also be investigated from cell membrane fragments overexpressing the receptor of interest, bypassing isolation and reconstitution procedures. The method is direct, sensitive, and does not rely on the use of any labeled material.

摘要

该研究的 G 蛋白偶联受体 (GPCR ) 的激活和信号转导机制的研究往往是孤立的, 纯化和重建 GPCR 模型脂质膜。从去污剂胶束系统重建 GPCR 到模型膜通常是一个艰苦的过程, 其成功与否是通过相当间接的方法来检测的, 如 SDS-PAGE 和 western blot 或通过生物物理方法。之后, 在另一个不同的实验装置中测量蛋白质的活性。总的来说, 整个过程是乏味的, 漫长的, 往往需要大量的材料和使用标记的蛋白质。本文描述了一种方案, 可以在单个实验装置中, 从去污剂胶束中重建 GPCR 到平面脂质双层, 并使用等离子体波导共振测量其配体结合活性。或者, 也可以从过表达感兴趣的受体的细胞膜片段中研究受体/配体相互作用, 从而绕过分离和重建过程。该方法是直接的, 敏感的, 不依赖于任何标记材料的使用。

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