Hariharan Parameswaran, Guan Lan
Dept of Cell Physiology and Molecular Biophysics, Center for Membrane Protein Research, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Bio Protoc. 2024 Aug 5;14(15):e5045. doi: 10.21769/BioProtoc.5045.
Membrane proteins play critical roles in cell physiology and pathology. The conventional way to study membrane proteins at protein levels is to use optimal detergents to extract proteins from membranes. Identification of the optimal detergent is tedious , and in some cases, the protein functions are compromised. While this detergent-based approach has produced meaningful results in membrane protein research, a lipid environment should be more suitable to recapture the protein's native folding and functions. This protocol describes how to prepare amphipathic membrane scaffold-proteins (MSPs)-based nanodiscs of a cation-coupled melibiose symporter of serovar Typhimurium (MelB), a member of the major facilitator superfamily. MSPs generate nano-assemblies containing membrane proteins surrounded by a patch of native lipids to better preserve their native conformations and functions. This protocol requires purified membrane protein in detergents, purified MSPs in solution, and detergent-destabilized phospholipids. The mixture of all three components at specific ratios is incubated in the presence of Bio-Beads SM-2 resins, which absorb all detergent molecules, allowing the membrane protein to associate with lipids surrounded by the MSPs. By reconstituting the purified membrane proteins back into their native-like lipid environment, these nanodisc-like particles can be directly used in cryo-EM single-particle analysis for structure determination and other biophysical analyses. It is noted that nanodiscs may potentially limit the dynamics of membrane proteins due to suboptimal nanodisc size compared to the native lipid bilayer. Key features • This protocol was built based on the method originally developed by Sligar et al. [1] and modified for a specific major facilitator superfamily transporter • This protocol is robust and reproducible • Lipid nanodiscs can increase membrane protein stability, and reconstituted transporters in lipid nanodiscs can regain function if their function is compromised using detergents • The reconstituted lipids nanodisc can be used for cryo-EM single-particle analysis.
膜蛋白在细胞生理和病理过程中发挥着关键作用。在蛋白质水平上研究膜蛋白的传统方法是使用最佳去污剂从膜中提取蛋白质。确定最佳去污剂的过程很繁琐,而且在某些情况下,蛋白质的功能会受到影响。虽然这种基于去污剂的方法在膜蛋白研究中取得了有意义的成果,但脂质环境应该更适合恢复蛋白质的天然折叠和功能。本方案描述了如何制备基于两亲性膜支架蛋白(MSP)的纳米盘,该纳米盘包含鼠伤寒血清型阳离子偶联蜜二糖转运体(MelB),它是主要促进剂超家族的成员。MSP会形成纳米组装体,其中包含被一片天然脂质包围的膜蛋白,从而更好地保留其天然构象和功能。本方案需要洗涤剂中的纯化膜蛋白、溶液中的纯化MSP以及洗涤剂不稳定的磷脂。将这三种成分按特定比例混合,在Bio-Beads SM-2树脂存在下孵育,Bio-Beads SM-2树脂会吸收所有洗涤剂分子,使膜蛋白与MSP包围的脂质结合。通过将纯化的膜蛋白重新构建回其类似天然的脂质环境中,这些类似纳米盘的颗粒可直接用于冷冻电镜单颗粒分析以确定结构以及进行其他生物物理分析。需要注意的是,与天然脂质双层相比,由于纳米盘尺寸不理想,纳米盘可能会潜在地限制膜蛋白的动力学。关键特性• 本方案基于Sligar等人最初开发的方法[1]构建,并针对特定的主要促进剂超家族转运体进行了修改• 本方案稳健且可重复• 脂质纳米盘可提高膜蛋白稳定性,并且如果使用洗涤剂使转运体功能受损,脂质纳米盘中重构的转运体可恢复功能• 重构的脂质纳米盘可用于冷冻电镜单颗粒分析。