Zuse Institute Berlin (ZIB).
IEEE Trans Vis Comput Graph. 2011 Dec;17(12):2025-34. doi: 10.1109/TVCG.2011.259.
Visual analysis is widely used to study the behavior of molecules. Of particular interest are the analysis of molecular interactions and the investigation of binding sites. For large molecules, however, it is difficult to detect possible binding sites and paths leading to these sites by pure visual inspection. In this paper, we present new methods for the computation and visualization of potential molecular paths. Using a novel filtering method, we extract the significant paths from the Voronoi diagram of spheres. For the interactive visualization of molecules and their paths, we present several methods using deferred shading and other state-of-the-art techniques. To allow for a fast overview of reachable regions of the molecule, we illuminate the molecular surface using a large number of light sources placed on the extracted paths. We also provide a method to compute the extension surface of selected paths and visualize it using the skin surface. Furthermore, we use the extension surface to clip the molecule to allow easy visual tracking of even deeply buried paths. The methods are applied to several proteins to demonstrate their usefulness.
可视化分析被广泛用于研究分子的行为。特别感兴趣的是分子相互作用的分析和结合部位的研究。然而,对于大型分子,通过纯目视检查很难检测到可能的结合部位和通往这些部位的路径。在本文中,我们提出了计算和可视化潜在分子路径的新方法。使用新颖的过滤方法,我们从球体的 Voronoi 图中提取重要路径。为了对分子及其路径进行交互式可视化,我们使用了几种使用延迟着色和其他最新技术的方法。为了能够快速概览分子的可达区域,我们使用放置在提取路径上的大量光源来照亮分子表面。我们还提供了一种计算选定路径的扩展曲面的方法,并使用皮肤曲面对其进行可视化。此外,我们使用扩展曲面裁剪分子,以允许轻松跟踪即使深埋的路径。该方法已应用于几种蛋白质,以证明其有用性。