Protein Structure Visualization by Dimension Reduction and Texture Mapping

Heng Yang, R. Qureshi, A. Sacan
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引用次数: 2

Abstract

Among the biological macromolecules, proteins have attracted special attention from the scientific community due to their rich functional roles. The ability to visualize and manipulate macromolecular structures on graphical display devices has facilitated the identification and analysis of these macromolecules. Structural analyses of the proteins often provide important insights into their biochemical functions. However, such analysis is often limited by the representation of protein structures and the corresponding computational resource requirements. In this study, we focus on the molecular surface of the proteins and investigate computationally and visually effective representations to serve a number of visualization and analysis purposes. Specifically, we "unfold" the protein surface onto a planar space, while preserving the local surface features as much as possible. In contrast to classical cartographic projections, our approach is able to preserve local shape features. Several biochemical properties associated with each surface point are mapped to generate a two dimensional map of these features. The 3D-2D mapping of the surface vertices has also been utilized to texture-map an arbitrary image back onto the protein structure to facilitate the visualization of the 3D structure.
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基于降维和纹理映射的蛋白质结构可视化
在生物大分子中,蛋白质因其丰富的功能作用而受到科学界的特别关注。在图形显示设备上可视化和操作大分子结构的能力促进了这些大分子的识别和分析。对蛋白质的结构分析通常提供对其生化功能的重要见解。然而,这种分析常常受到蛋白质结构的表示和相应的计算资源要求的限制。在这项研究中,我们专注于蛋白质的分子表面,并研究计算和视觉上有效的表示,以服务于许多可视化和分析目的。具体来说,我们将蛋白质表面“展开”到一个平面空间,同时尽可能地保留局部表面特征。与传统的地图投影相比,我们的方法能够保留局部形状特征。与每个表面点相关的几个生化特性被映射以生成这些特征的二维地图。表面顶点的3D- 2d映射也被用于将任意图像纹理映射回蛋白质结构上,以促进3D结构的可视化。
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