Zhu Y, Carragher B, Kriegman D J, Milligan R A, Potter C S
Beckman Institute, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
J Struct Biol. 2001 Sep;135(3):302-12. doi: 10.1006/jsbi.2001.4415.
Since the foundation for the three-dimensional image reconstruction of helical objects from electron micrographs was laid more than 30 years ago, there have been sustained developments in specimen preparation, data acquisition, image analysis, and interpretation of results. However, the boxing of filaments in large numbers of images--one of the critical steps toward the reconstruction at high resolution--is still constrained by manual processing even though interactive interfaces have been built to aid the tedious and sometimes inaccurate boxing process. This article describes an accurate approach for automated detection of filamentous structures in low-contrast images acquired in defocus pairs using cryoelectron microscopy. The performance of the approach has been evaluated across various magnifications and at a series of defocus values using tobacco mosaic virus (TMV) preserved in vitreous ice as a test specimen. By integrating the proposed approach into our automated data acquisition and reconstruction system, we are now able to generate a three-dimensional map of TMV to approximately 10-A resolution within 24 h of inserting the specimen grid into the microscope.
自从三十多年前奠定了从电子显微照片进行螺旋物体三维图像重建的基础以来,在样品制备、数据采集、图像分析以及结果解读方面都取得了持续进展。然而,即使已经构建了交互式界面来辅助这一繁琐且有时不准确的框选过程,但在大量图像中对细丝进行框选——这是高分辨率重建的关键步骤之一——仍受手工处理的限制。本文描述了一种用于在使用冷冻电子显微镜以散焦对采集的低对比度图像中自动检测丝状结构的精确方法。使用保存在玻璃冰中的烟草花叶病毒(TMV)作为测试样品,在各种放大倍数和一系列散焦值下对该方法的性能进行了评估。通过将所提出的方法集成到我们的自动数据采集和重建系统中,我们现在能够在将样品网格插入显微镜后的24小时内生成分辨率约为10埃的TMV三维图谱。