Accurate magnification determination for cryoEM using gold

IF 2.1 3区 工程技术 Q2 MICROSCOPY Ultramicroscopy Pub Date : 2023-11-15 DOI:10.1016/j.ultramic.2023.113883
Joshua L. Dickerson, Erin Leahy, Mathew J. Peet, Katerina Naydenova, Christopher J. Russo
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Abstract

Determining the correct magnified pixel size of single-particle cryoEM micrographs is necessary to maximize resolution and enable accurate model building. Here we describe a simple and rapid procedure for determining the absolute magnification in an electron cryomicroscope to a precision of <0.5%. We show how to use the atomic lattice spacings of crystals of thin and readily available test specimens, such as gold, as an absolute reference to determine magnification for both room temperature and cryogenic imaging. We compare this method to other commonly used methods, and show that it provides comparable accuracy in spite of its simplicity. This magnification calibration method provides a definitive reference quantity for data analysis and processing, simplifies the combination of multiple datasets from different microscopes and detectors, and improves the accuracy with which the contrast transfer function of the microscope can be determined. We also provide an open source program, magCalEM, which can be used to accurately estimate the magnified pixel size of a cryoEM dataset ex post facto.

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用金测定冷冻电镜的精确放大倍率
确定正确的放大像素大小的单粒子低温显微镜是必要的,以最大限度地提高分辨率,使准确的模型建设。在这里,我们描述了一种简单而快速的程序,用于确定电子冷冻显微镜的绝对放大倍率,其精度为0.5%。我们展示了如何使用薄晶体的原子晶格间距和容易获得的测试样品,如金,作为确定室温和低温成像放大倍率的绝对参考。我们将这种方法与其他常用的方法进行比较,并表明,尽管它简单,但它提供了相当的准确性。该方法为数据分析和处理提供了明确的参考量,简化了不同显微镜和检测器的多组数据集的组合,提高了确定显微镜对比度传递函数的准确性。我们还提供了一个开源程序magCalEM,它可以用来准确地估计冷冻em数据集的放大像素大小。
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来源期刊
Ultramicroscopy
Ultramicroscopy 工程技术-显微镜技术
CiteScore
4.60
自引率
13.60%
发文量
117
审稿时长
5.3 months
期刊介绍: Ultramicroscopy is an established journal that provides a forum for the publication of original research papers, invited reviews and rapid communications. The scope of Ultramicroscopy is to describe advances in instrumentation, methods and theory related to all modes of microscopical imaging, diffraction and spectroscopy in the life and physical sciences.
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