Leo Jack C, Oberhettinger Philipp, Linke Dirk
Department of Biosciences, University of Oslo, Oslo, 0316, Norway.
Interfaculty Institute for Microbiology and Infection Medicine, University Clinics Tübingen, Tübingen, Germany.
Methods Mol Biol. 2015;1329:157-67. doi: 10.1007/978-1-4939-2871-2_12.
In addition to the cytoplasmic membrane, Gram-negative bacteria have a second lipid bilayer, the outer membrane, which is the de facto barrier between the cell and the extracellular milieu. Virtually all integral proteins of the outer membrane form β-barrels, which are inserted into the outer membrane by the BAM complex. Some outer membrane proteins, like the porins and trimeric autotransporter adhesins, are multimeric. In the former case, the porin trimer consists of three individual β-barrels, whereas in the latter, the single autotransporter β-barrel domain is formed by three separate polypeptides. This chapter reviews methods to investigate the folding and membrane insertion of multimeric OMPs and further explains the use of a BamA depletion strain to study the effects of the BAM complex on multimeric OMPs in E. coli.
除细胞质膜外,革兰氏阴性菌还有第二个脂质双层膜,即外膜,它实际上是细胞与细胞外环境之间的屏障。外膜的几乎所有整合蛋白都形成β桶状结构,这些结构由BAM复合物插入外膜。一些外膜蛋白,如孔蛋白和三聚体自转运黏附素,是多聚体。在前一种情况下,孔蛋白三聚体由三个单独的β桶状结构组成,而在后一种情况下,单个自转运β桶状结构域由三个独立的多肽形成。本章综述了研究多聚体外膜蛋白折叠和膜插入的方法,并进一步解释了使用BamA缺失菌株来研究BAM复合物对大肠杆菌中多聚体外膜蛋白的影响。