Nilsson I, Witt S, Kiefer H, Mingarro I, von Heijne G
Department of Biochemistry, Stockholm University, S-10691 Stockholm, Sweden.
J Biol Chem. 2000 Mar 3;275(9):6207-13. doi: 10.1074/jbc.275.9.6207.
We have studied the membrane insertion of ProW, an Escherichia coli inner membrane protein with seven transmembrane segments and a large periplasmic N-terminal tail, into endoplasmic reticulum (ER)-derived dog pancreas microsomes. Strikingly, significant levels of N-tail translocation is seen only when a minimum of four of the transmembrane segments are present; for constructs with fewer transmembrane segments, the N-tail remains mostly nontranslocated and the majority of the molecules adopt an "inverted" topology where normally nontranslocated parts are translocated and vice versa. N-tail translocation can also be promoted by shortening of the N-tail and by the addition of positively charged residues immediately downstream of the first trasnmembrane segment. We conclude that as many as four consecutive transmembrane segments may be collectively involved in determining membrane protein topology in the ER and that the effects of downstream sequence determinants may vary depending on the size and charge of the N-tail. We also provide evidence to suggest that the ProW N-tail is translocated across the ER membrane in a C-to-N-terminal direction.
我们研究了ProW(一种具有七个跨膜区段和一个大的周质N末端尾巴的大肠杆菌内膜蛋白)插入内质网(ER)来源的犬胰腺微粒体中的膜插入情况。令人惊讶的是,只有当至少存在四个跨膜区段时,才会观察到显著水平的N末端尾巴转运;对于跨膜区段较少的构建体,N末端尾巴大多仍未转运,并且大多数分子采用“反向”拓扑结构,即通常未转运的部分发生转运,反之亦然。缩短N末端尾巴以及在第一个跨膜区段下游紧邻添加带正电荷的残基也可以促进N末端尾巴的转运。我们得出结论,多达四个连续的跨膜区段可能共同参与确定ER中膜蛋白的拓扑结构,并且下游序列决定因素的影响可能因N末端尾巴的大小和电荷而异。我们还提供证据表明ProW的N末端尾巴以C端到N端的方向穿过ER膜。