Conway J F, Trus B L, Booy F P, Newcomb W W, Brown J C, Steven A C
Laboratory of Structural Biology, National Institute of Arthritis, Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Struct Biol. 1996 Jan-Feb;116(1):200-8. doi: 10.1006/jsbi.1996.0031.
Full evaluation of three-dimensional density maps calculated from cryoelectron micrographs of complex supramolecular structures requires that the maps be sifted by a variety of complementary visualization techniques. We present here a primer for a number of such techniques in current widespread use, including surface rendering; serial sections; simulated motion; and real-time manipulation of tiled surfaces displayed on an advanced workstation. The principles on which these techniques operate are briefly reviewed, as are their advantages and limitations, with emphasis on the requirements for visual representation of viral capsid structures. These methods are illustrated in application to a density map of herpes simplex virus type 1 (HSV-1) capsid at 24 A resolution, which reveals more detailed information than heretofore concerning the inner surface of the icosahedral capsid shell and the 150-A-long channels that pass through each of the 162 capsomers.
对由复杂超分子结构的冷冻电子显微照片计算得到的三维密度图进行全面评估,需要通过多种互补的可视化技术对这些图进行筛选。我们在此介绍一些当前广泛使用的此类技术的入门知识,包括表面渲染;连续切片;模拟运动;以及在先进工作站上对平铺表面进行实时操作。简要回顾了这些技术所基于的原理,以及它们的优点和局限性,重点是病毒衣壳结构视觉呈现的要求。这些方法应用于分辨率为24埃的单纯疱疹病毒1型(HSV-1)衣壳的密度图进行了说明,该密度图揭示了比以往更多关于二十面体衣壳壳体内表面以及穿过162个衣壳粒中每一个的150埃长通道的详细信息。