Biozentrum, University of Basel, Basel, Switzerland.
Methods Mol Biol. 2020;2127:373-396. doi: 10.1007/978-1-0716-0373-4_24.
NMR spectroscopy is a method of choice to characterize structure, function, and dynamics of integral membrane proteins at atomic resolution. Here, we describe protocols for sample preparation and characterization by NMR spectroscopy of two integral membrane proteins with different architecture, the α-helical membrane protein MsbA and the β-barrel membrane protein BamA. The protocols describe recombinant expression in E. coli, protein refolding, purification, and reconstitution in suitable membrane mimetics, as well as key setup steps for basic NMR experiments. These include experiments on protein samples in the solid state under magic angle spinning (MAS) conditions and experiments on protein samples in aqueous solution. Since MsbA and BamA are typical examples of their respective architectural classes, the protocols presented here can also serve as a reference for other integral membrane proteins.
NMR 光谱学是一种选择,用于在原子分辨率下表征整体膜蛋白的结构、功能和动力学。在这里,我们描述了通过 NMR 光谱学对两种具有不同结构的整体膜蛋白(α-螺旋膜蛋白 MsbA 和 β-桶膜蛋白 BamA)进行样品制备和表征的方案。该方案描述了在大肠杆菌中的重组表达、蛋白质重折叠、在合适的膜类似物中的纯化和重组,以及基本 NMR 实验的关键设置步骤。这些实验包括在魔角旋转(MAS)条件下的固态蛋白样品实验和在水溶液中的蛋白样品实验。由于 MsbA 和 BamA 是各自结构类别的典型代表,因此这里提出的方案也可以作为其他整体膜蛋白的参考。