Stoenescu Roxana, Graff Alexandra, Meier Wolfgang
Department of Chemistry, University of Basel, Klingelbergstr. 80, CH-4056 Basel, Switzerland.
Macromol Biosci. 2004 Oct 20;4(10):930-5. doi: 10.1002/mabi.200400065.
Asymmetric molecules and materials provide an important basis for the organization and function of biological systems. It is well known that, for example, the inner and outer leaflets of biological membranes are strictly asymmetric with respect to lipid composition and distribution. This plays a crucial role for many membrane-related processes like carrier-mediated transport or insertion and orientation of integral membrane proteins. Most artificial membrane systems are, however, symmetric with respect to their midplane and membrane proteins are incorporated with random orientation. Here we describe a new approach to induce a directed insertion of membrane proteins into asymmetric membranes formed by amphiphilic ABC triblock copolymers with two chemically different water-soluble blocks A and C. In a comparative study we have reconstituted His-tag labeled Aquaporin 0 in lipid, ABA block copolymer, and ABC block copolymer vesicles. Immunolabeling, colorimetric, and fluorescence studies clearly show that a preferential orientation of the protein is only observed in the asymmetric ABC triblock copolymer membranes.
不对称分子和材料为生物系统的组织和功能提供了重要基础。例如,众所周知,生物膜的内外小叶在脂质组成和分布方面严格不对称。这对许多与膜相关的过程起着关键作用,如载体介导的运输或整合膜蛋白的插入和取向。然而,大多数人工膜系统相对于其中心平面是对称的,并且膜蛋白以随机取向掺入。在这里,我们描述了一种新方法,可诱导膜蛋白定向插入由具有两个化学不同的水溶性嵌段A和C的两亲性ABC三嵌段共聚物形成的不对称膜中。在一项比较研究中,我们在脂质、ABA嵌段共聚物和ABC嵌段共聚物囊泡中重组了His标签标记的水通道蛋白0。免疫标记、比色和荧光研究清楚地表明,仅在不对称ABC三嵌段共聚物膜中观察到蛋白质的优先取向。