European Molecular Biology Laboratory Hamburg, Hamburg, Germany.
Centre for Structural Systems Biology (CSSB), Hamburg, Germany.
Methods Mol Biol. 2023;2652:215-230. doi: 10.1007/978-1-0716-3147-8_12.
Membrane proteins are responsible for a large variety of tasks in organisms and of particular interesting as drug targets. At the same time, they are notoriously difficult to work with and require a thorough characterization before proceeding with structural studies. Here, we present a biophysical pipeline to characterize membrane proteins focusing on the optimization of stability, aggregation behavior, and homogeneity. The pipeline shown here is built on three biophysical techniques: differential scanning fluorimetry using native protein fluorescence (nano differential scanning fluorimetry), dynamic light scattering, and mass photometry. For each of these techniques, we provide detailed protocols for performing experiments and data analysis.
膜蛋白在生物体中负责多种任务,并且作为药物靶点特别有趣。同时,它们非常难以处理,在进行结构研究之前需要进行彻底的表征。在这里,我们提出了一个生物物理管道来表征膜蛋白,重点是优化稳定性、聚集行为和均一性。这里展示的管道建立在三种生物物理技术的基础上:使用天然蛋白质荧光的差示扫描荧光法(纳米差示扫描荧光法)、动态光散射和质量光度法。对于这些技术中的每一种,我们都提供了执行实验和数据分析的详细协议。