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微尺度热泳法评估异源过表达膜蛋白在膜制剂中的功能。

Microscale Thermophoresis to Evaluate the Functionality of Heterologously Overexpressed Membrane Proteins in Membrane Preparations.

机构信息

Université Côte d'Azur, CNRS UMR 7275, Institut de Pharmacologie Moléculaire et Cellulaire , Valbonne, France.

NanoTemper Technologies GmbH, Munich, Germany.

出版信息

Methods Mol Biol. 2022;2507:445-461. doi: 10.1007/978-1-0716-2368-8_24.

Abstract

Transmembrane proteins are challenging to express in heterologous systems and to purify, thus any technique enabling to evaluate the functionality of the protein produced prior purification provides a huge step forward. Furthermore, the membrane environment may be critical for the activity of the target protein and accessing information in the membrane fragments instead of solubilizing the target into a detergent that may be unsuitable for its function is key to study and evaluate its activity. Herein, we describe how microscale thermophoresis (MST) was used to evaluate the functionality of membrane proteins directly in host membrane preparation before purification. We give a protocol to measure the affinity between the human Hedgehog (Hh) receptor Ptch1 in yeast plasma membrane and the small molecule PAH, which was shown to inhibit its drug efflux activity.

摘要

跨膜蛋白在异源系统中表达和纯化具有挑战性,因此任何能够在纯化前评估所产生蛋白质功能的技术都向前迈进了一大步。此外,膜环境可能对靶蛋白的活性至关重要,而直接在宿主膜制剂中访问膜片段中的信息而不是将靶蛋白溶解在可能不适合其功能的去污剂中是研究和评估其活性的关键。本文中,我们描述了如何在纯化前使用微量热泳动(MST)直接在宿主膜制剂中评估膜蛋白的功能。我们提供了一种方案来测量人 Hedgehog(Hh)受体 Ptch1 在酵母质膜中和小分子 PAH 之间的亲和力,该亲和力被证明能抑制其药物外排活性。

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