Kiefer Dorothee, Kuhn Andreas
Department of Microbiology, University of Hohenheim, D-70599 Stuttgart, Germany.
Int Rev Cytol. 2007;259:113-38. doi: 10.1016/S0074-7696(06)59003-5.
Membrane proteins fulfill a number of vital functions in prokaryotic and eukaryotic cells. They are often organized in multicomponent complexes, folded within the membrane bilayer and interacting with the cytoplasmic and periplasmic or external soluble compartments. For the biogenesis of integral membrane proteins, the essential biochemical steps are (1) the insertion and topogenesis of the transmembrane protein segments into the lipid bilayer, (2) the three-dimensional folding of the translocated hydrophilic domains, and (3) the assembly into multimeric complexes. Intensive research has elucidated the basic mechanisms of membrane protein insertion in the homologous translocation machineries of different cellular systems. Whereas the Sec translocation system is found in the endoplasmic reticulum of eukaryotic cells and in the prokaryotic plasma membrane, the YidC-Oxa1 membrane insertase is present in prokaryotic and organellar membranes. This review focuses on the discoveries of the YidC system in bacterial as well as the Oxa1/Alb3 protein family of eukaryotic cells and will particularly emphasize evolutionary aspects.
膜蛋白在原核细胞和真核细胞中发挥着许多重要功能。它们通常组装成多组分复合物,折叠于膜双层中,并与细胞质、周质或外部可溶性区室相互作用。对于整合膜蛋白的生物合成,基本的生化步骤包括:(1)跨膜蛋白片段插入脂质双层并进行拓扑定位;(2)易位的亲水区进行三维折叠;(3)组装成多聚体复合物。深入研究已阐明了膜蛋白在不同细胞系统同源转运机制中的插入基本机制。真核细胞内质网和原核细胞质膜中存在Sec转运系统,而YidC - Oxa1膜插入酶存在于原核生物和细胞器膜中。本综述着重介绍细菌中YidC系统以及真核细胞中Oxa1/Alb3蛋白家族的发现,并特别强调进化方面的内容。