Gafvelin G, Sakaguchi M, Andersson H, von Heijne G
Department of Biochemistry, Stockholm University, S-106 91 Stockholm, Sweden.
J Biol Chem. 1997 Mar 7;272(10):6119-27. doi: 10.1074/jbc.272.10.6119.
Insertion into the endoplasmic reticulum membrane of model proteins with one, two, and four transmembrane segments and different distributions of positively charged residues in the N-terminal tail and the polar loops has been studied both in vitro and in vivo. Membrane insertion of these same constructs has previously been analyzed in Escherichia coli, thus making possible a detailed comparison between the topological rules for membrane protein assembly in prokaryotic and eukaryotic cells. In general, we find that positively charged residues have similar effects on the membrane topology in both systems when they are placed in the N-terminal tail but that the effects of charged residues in internal loops clearly differ. Our results rule out a sequential start-stop transfer model where successive hydrophobic segments insert with alternating orientations starting from the most N-terminal one as the only mechanism for membrane protein insertion in eukaryotic cells.
对具有一、二和四个跨膜片段且在N端尾部和极性环中带正电残基分布不同的模型蛋白插入内质网膜的过程进行了体内和体外研究。此前已在大肠杆菌中分析过这些相同构建体的膜插入情况,从而能够详细比较原核细胞和真核细胞中膜蛋白组装的拓扑规则。总体而言,我们发现当带正电残基位于N端尾部时,它们在两个系统中对膜拓扑结构具有相似的影响,但内部环中带电残基的影响明显不同。我们的结果排除了一种顺序性的起始-终止转移模型,即连续的疏水片段从最N端的片段开始以交替方向插入,作为真核细胞中膜蛋白插入的唯一机制。