Thuman-Commike P A
QED Labs, 1190 S. Bascom Ave., Suite 208, San Jose, CA 95128, USA.
FEBS Lett. 2001 Sep 14;505(2):199-205. doi: 10.1016/s0014-5793(01)02804-6.
Three-dimensional structure determination of macromolecules and macromolecular complexes is an integral part of understanding biological functions. For large protein and macromolecular complexes structure determination is often performed using electron cryomicroscopy where projection images of individual macromolecular complexes are combined to produce a three-dimensional reconstruction. Single particle methods have been devised to perform this structure determination for macromolecular complexes with little or no underlying symmetry. These computational methods generally involve an iterative process of aligning unique views of the macromolecular images followed by determination of the angular components that define those views. In this review, this structure determination process is described with the aim of clarifying a seemingly complex structural method.
大分子和大分子复合物的三维结构测定是理解生物学功能不可或缺的一部分。对于大型蛋白质和大分子复合物,结构测定通常使用电子冷冻显微镜进行,其中单个大分子复合物的投影图像被组合起来以产生三维重建。已经设计出单颗粒方法来对几乎没有或没有基本对称性的大分子复合物进行这种结构测定。这些计算方法通常涉及一个迭代过程,即对齐大分子图像的独特视图,然后确定定义这些视图的角度分量。在这篇综述中,描述了这种结构测定过程,目的是阐明一种看似复杂的结构方法。