Shu Sheng, Mi Wei
Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06520, USA.
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.
Bio Protoc. 2023 Mar 20;13(6):e4638. doi: 10.21769/BioProtoc.4638.
an outer membrane (OM), a peptidoglycan cell wall, and an inner membrane (IM). The OM and IM have different components of proteins and lipids. Separating the IM and OM is a basic biochemical procedure to further study lipids and membrane proteins in different locations. Sucrose gradient ultracentrifugation of lysozyme/EDTA-treated total membrane is the most widely used method to separate the IM and OM of Gram-negative bacteria. However, EDTA is often harmful to protein structure and function. Here, we describe a relatively simple sucrose gradient ultracentrifugation method to separate the IM and OM of Escherichia coli. In this method, the cells are broken by a high-pressure microfluidizer, and the total cell membrane is collected by ultracentrifugation. The IM and OM are then separated on a sucrose gradient. Because EDTA is not used, this method is beneficial for subsequent membrane protein purification and functional study.
外膜(OM)、肽聚糖细胞壁和内膜(IM)。外膜和内膜具有不同的蛋白质和脂质成分。分离内膜和外膜是进一步研究不同位置脂质和膜蛋白的基本生化步骤。对溶菌酶/乙二胺四乙酸(EDTA)处理的总膜进行蔗糖梯度超速离心是分离革兰氏阴性菌内膜和外膜最广泛使用的方法。然而,EDTA通常对蛋白质结构和功能有害。在此,我们描述一种相对简单的蔗糖梯度超速离心方法来分离大肠杆菌的内膜和外膜。在该方法中,细胞通过高压微射流破碎,总细胞膜通过超速离心收集。然后在内膜和外膜在蔗糖梯度上进行分离。由于未使用EDTA,该方法有利于后续膜蛋白的纯化和功能研究。