Yoshioka Craig, Pulokas James, Fellmann Denis, Potter Clinton S, Milligan Ronald A, Carragher Bridget
The National Resource for Automated Molecular Microscopy, Department of Cell Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
J Struct Biol. 2007 Sep;159(3):335-46. doi: 10.1016/j.jsb.2007.03.005. Epub 2007 Apr 20.
Visualization by electron microscopy has provided many insights into the composition, quaternary structure, and mechanism of macromolecular assemblies. By preserving samples in stain or vitreous ice it is possible to image them as discrete particles, and from these images generate three-dimensional structures. This 'single-particle' approach suffers from two major shortcomings; it requires an initial model to reconstitute 2D data into a 3D volume, and it often fails when faced with conformational variability. Random conical tilt (RCT) and orthogonal tilt (OTR) are methods developed to overcome these problems, but the data collection required, particularly for vitreous ice specimens, is difficult and tedious. In this paper, we present an automated approach to RCT/OTR data collection that removes the burden of manual collection and offers higher quality and throughput than is otherwise possible. We show example datasets collected under stain and cryo conditions and provide statistics related to the efficiency and robustness of the process. Furthermore, we describe the new algorithms that make this method possible, which include new calibrations, improved targeting and feature-based tracking.
电子显微镜可视化技术为深入了解大分子组装体的组成、四级结构和机制提供了诸多见解。通过将样品保存在染色剂或玻璃态冰中,可以将它们成像为离散颗粒,并从这些图像生成三维结构。这种“单颗粒”方法存在两个主要缺点:它需要一个初始模型来将二维数据重建为三维体积,并且在面对构象变异性时常常失败。随机圆锥倾斜(RCT)和正交倾斜(OTR)是为克服这些问题而开发的方法,但所需的数据采集,特别是对于玻璃态冰标本,既困难又繁琐。在本文中,我们提出了一种用于RCT/OTR数据采集的自动化方法,该方法消除了手动采集的负担,并提供了比其他方式更高的质量和通量。我们展示了在染色和冷冻条件下收集的示例数据集,并提供了与该过程的效率和稳健性相关的统计数据。此外,我们描述了使该方法成为可能的新算法,其中包括新的校准、改进的靶向和基于特征的跟踪。