National Resource for Automated Molecular Microscopy and Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
J Struct Biol. 2010 Mar;169(3):389-98. doi: 10.1016/j.jsb.2009.12.005. Epub 2009 Dec 16.
Structure determination of a novel macromolecular complex via single-particle electron microscopy depends upon overcoming the challenge of establishing a reliable 3-D reconstruction using only 2-D images. There are a variety of strategies that deal with this issue, but not all of them are readily accessible and straightforward to use. We have developed a "toolbox" of ab initio reconstruction techniques that provide several options for calculating 3-D volumes in an easily managed and tightly controlled work-flow that adheres to standard conventions and formats. This toolbox is designed to streamline the reconstruction process by removing the necessity for bookkeeping, while facilitating transparent data transfer between different software packages. It currently includes procedures for calculating ab initio reconstructions via random or orthogonal tilt geometry, tomograms, and common lines, all of which have been tested using the 50S ribosomal subunit. Our goal is that the accessibility of multiple independent reconstruction algorithms via this toolbox will improve the ease with which models can be generated, and provide a means of evaluating the confidence and reliability of the final reconstructed map.
通过单颗粒电子显微镜确定新型大分子复合物的结构取决于克服仅使用 2D 图像建立可靠 3D 重建的挑战。有多种策略可以解决这个问题,但并非所有策略都易于使用。我们开发了一套从头开始重建技术的“工具箱”,这些技术提供了几种选项,可以在易于管理和严格控制的工作流程中计算 3D 体积,该流程符合标准惯例和格式。该工具箱旨在通过消除簿记的必要性来简化重建过程,同时促进不同软件包之间透明的数据传输。它目前包括通过随机或正交倾斜几何、断层扫描和公共线计算从头开始重建的程序,所有这些都已使用 50S 核糖体亚基进行了测试。我们的目标是,通过这个工具箱可以访问多种独立的重建算法,这将提高生成模型的便利性,并提供一种评估最终重建地图的置信度和可靠性的方法。