Sosa H, Milligan R A
Department of Cell Biology, Scripps Research Institute, La Jolla, CA 92037, USA.
J Mol Biol. 1996 Aug 2;260(5):743-55. doi: 10.1006/jmbi.1996.0434.
We have used cryo-electron microscopy and image analysis to obtain the three-dimensional (3D) structure of 11, 12, 14 and 15 protofilament microtubules decorated with the motor domain of ncd. To obtain the 3D maps, we developed a back-projection method that does not require a helical arrangement of the tubulin heterodimers. This method allows the calculation of 3D maps even when lattice discontinuities (seams) are present. The maps show that the microtubules we studied conform to a B-type lattice with one or more seams. In the presence of 5'-adenylim-idodiphosphate (AMP-PNP), the motor domain of ncd binds to the microtubule protofilament crest interacting with only one protofilament. Viewing the structures along the microtubule axis shows that the ncd motor domain and the tubulin are titled in opposite directions. We determined that a clockwise tilt of the tubulin subunits corresponds to a view from the minus end towards the plus end of the microtubule.
我们利用冷冻电子显微镜和图像分析技术,获得了由ncd运动结构域修饰的11、12、14和15根原纤维微管的三维(3D)结构。为了获得3D图谱,我们开发了一种无需微管蛋白异二聚体呈螺旋排列的反投影方法。即使存在晶格不连续性(缝隙),该方法也能计算出3D图谱。这些图谱表明,我们研究的微管符合具有一个或多个缝隙的B型晶格。在5'-腺苷酰亚胺二磷酸(AMP-PNP)存在的情况下,ncd的运动结构域与微管原纤维嵴结合,仅与一根原纤维相互作用。沿微管轴观察结构表明,ncd运动结构域和微管蛋白的倾斜方向相反。我们确定微管蛋白亚基的顺时针倾斜对应于从微管负端向正端的视角。