Electrical Engineering and Computer Science, MIT, Cambridge, MA 02139, USA.
J Struct Biol. 2010 Jun;170(3):427-38. doi: 10.1016/j.jsb.2010.03.007. Epub 2010 Mar 23.
Cryo-electron microscopy produces 3D density maps of molecular machines, which consist of various molecular components such as proteins and RNA. Segmentation of individual components in such maps is a challenging task, and is mostly accomplished interactively. We present an approach based on the immersive watershed method and grouping of the resulting regions using progressively smoothed maps. The method requires only three parameters: the segmentation threshold, a smoothing step size, and the number of smoothing steps. We first apply the method to maps generated from molecular structures and use a quantitative metric to measure the segmentation accuracy. The method does not attain perfect accuracy, however it produces single or small groups of regions that roughly match individual proteins or subunits. We also present two methods for fitting of structures into density maps, based on aligning the structures with single regions or small groups of regions. The first method aligns centers and principal axes, whereas the second aligns centers and then rotates the structure to find the best fit. We describe both interactive and automated ways of using these two methods. Finally, we show segmentation and fitting results for several experimentally-obtained density maps.
低温电子显微镜产生分子机器的 3D 密度图,这些分子机器由各种分子成分组成,如蛋白质和 RNA。在这样的图谱中对单个成分进行分割是一项具有挑战性的任务,并且主要通过交互方式完成。我们提出了一种基于沉浸式分水岭方法的方法,并使用逐渐平滑的图谱对得到的区域进行分组。该方法仅需要三个参数:分割阈值、平滑步长和平滑步骤数。我们首先将该方法应用于由分子结构生成的图谱,并使用定量指标来测量分割准确性。然而,该方法并未达到完美的准确性,它只是产生大致匹配单个蛋白质或亚基的单个或小区域组。我们还提出了两种基于将结构与单个区域或小区域组对齐的方法来将结构拟合到密度图中。第一种方法对齐中心和主轴,而第二种方法则先对齐中心,然后旋转结构以找到最佳拟合。我们描述了这两种方法的交互和自动化使用方式。最后,我们展示了几个实验获得的密度图谱的分割和拟合结果。