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用于电子冷冻显微镜的 10k×10k CCD 的实际性能评估。

Practical performance evaluation of a 10k × 10k CCD for electron cryo-microscopy.

机构信息

Graduate Program in Structural and Computational Biology and Molecular Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

J Struct Biol. 2011 Sep;175(3):384-93. doi: 10.1016/j.jsb.2011.05.012. Epub 2011 May 17.

DOI:10.1016/j.jsb.2011.05.012
PMID:21619932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3150461/
Abstract

Electron cryo-microscopy (cryo-EM) images are commonly collected using either charge-coupled devices (CCD) or photographic film. Both film and the current generation of 16 megapixel (4k × 4k) CCD cameras have yielded high-resolution structures. Yet, despite the many advantages of CCD cameras, more than two times as many structures of biological macromolecules have been published in recent years using photographic film. The continued preference to film, especially for subnanometer-resolution structures, may be partially influenced by the finer sampling and larger effective specimen imaging area offered by film. Large format digital cameras may finally allow them to overtake film as the preferred detector for cryo-EM. We have evaluated a 111-megapixel (10k × 10k) CCD camera with a 9 μm pixel size. The spectral signal-to-noise ratios of low dose images of carbon film indicate that this detector is capable of providing signal up to at least 2/5 Nyquist frequency potentially retrievable for 3D reconstructions of biological specimens, resulting in more than double the effective specimen imaging area of existing 4k × 4k CCD cameras. We verified our estimates using frozen-hydrated ε15 bacteriophage as a biological test specimen with previously determined structure, yielding a ∼7 Å resolution single particle reconstruction from only 80 CCD frames. Finally, we explored the limits of current CCD technology by comparing the performance of this detector to various CCD cameras used for recording data yielding subnanometer resolution cryo-EM structures submitted to the electron microscopy data bank (http://www.emdatabank.org/).

摘要

电子冷冻透射显微镜(cryo-EM)图像通常使用电荷耦合器件(CCD)或照相胶片进行采集。照相胶片和当前一代的 1600 万像素(4k×4k)CCD 相机都已经获得了高分辨率结构。然而,尽管 CCD 相机具有许多优势,但近年来使用照相胶片发表的生物大分子结构的数量仍然超过了两倍。尽管 CCD 相机具有许多优势,但照相胶片的持续偏好,特别是对于亚纳米分辨率结构,可能部分受到照相胶片提供的更精细的采样和更大的有效样本成像面积的影响。大格式数码相机最终可能会使它们超过照相胶片,成为 cryo-EM 的首选探测器。我们评估了一款具有 9μm 像素尺寸的 1.11 亿像素(10k×10k)CCD 相机。碳膜低剂量图像的光谱信噪比表明,该探测器能够提供至少 2/5 奈奎斯特频率的信号,这对于生物样本的 3D 重建是可恢复的,从而使有效样本成像面积比现有的 4k×4k CCD 相机增加了一倍以上。我们使用先前确定结构的冷冻水合 ε15 噬菌体作为生物测试样本,验证了我们的估计,仅从 80 个 CCD 帧中就获得了约 7Å分辨率的单颗粒重建。最后,我们通过比较该探测器与用于记录获得 submarnometer 分辨率 cryo-EM 结构的各种 CCD 相机的性能,探索了当前 CCD 技术的极限,这些 cryo-EM 结构已提交给电子显微镜数据库(http://www.emdatabank.org/)。

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