Lücken U, Gogol E P, Capaldi R A
Institute of Molecular Biology, University of Oregon, Eugene 97403.
Biochemistry. 1990 Jun 5;29(22):5339-43. doi: 10.1021/bi00474a019.
The structural relationship of the catalytic portion (ECF1) of the Escherichia coli F1F0 ATP synthase (ECF1F0) to the intact, membrane-bound complex has been determined by cryoelectron microscopy and image analysis of single, unordered particles. ECF1F0, reconstituted into membrane structures, has been preserved and examined in its native state in a layer of amorphous ice. Side views of the ECF1F0 show the same elongated bilobed and trilobed projection of the ECF1 views shown previously to be normal to the hexagonal projection. The elongated aqueous cavity of the ECF1 is perpendicular to the membrane bilayer profile in the bilobed view. ECF1 is separated from the membrane-embedded F0 by a narrow stalk approximately 40 A long and approximately 25-30 A thick. The F0 part extends from the lipid bilayer by approximately 10 A on the side facing the ECF1. There is no clear extension of the protein on the opposite side of the membrane.
通过对单个无序颗粒进行冷冻电子显微镜观察和图像分析,确定了大肠杆菌F1F0 ATP合酶(ECF1F0)的催化部分(ECF1)与完整的膜结合复合物之间的结构关系。重新构建到膜结构中的ECF1F0在非晶冰层中以其天然状态保存并进行了检查。ECF1F0的侧视图显示出与先前所示的垂直于六边形投影的ECF1视图相同的细长双叶和三叶投影。在双叶视图中,ECF1的细长水腔垂直于膜双层轮廓。ECF1通过一个长约40埃、厚约25 - 30埃的狭窄茎与嵌入膜中的F0分离。F0部分在面向ECF1的一侧从脂质双层延伸约10埃。在膜的另一侧没有明显的蛋白质延伸。