利用 Gatan Alpine 直接电子探测器进行 100-200 千伏的高分辨率单粒子成像。

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lieza M. Chan , Brandon J. Courteau , Allison Maker , Mengyu Wu , Benjamin Basanta , Hev Mehmood , David Bulkley , David Joyce , Brian C. Lee , Stephen Mick , Cory Czarnik , Sahil Gulati , Gabriel C. Lander , Kliment A. Verba
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引用次数: 0

摘要

直接电子探测器技术的发展在利用低温电子显微镜进行 200 和 300 千伏高分辨率结构研究方面发挥了关键作用。然而,理论和最近的实验表明,在 100 keV 的能量下成像具有优势,而目前的探测器尚未针对该能量进行优化。在这项研究中,我们评估了专为在 100 和 200 keV 下工作而设计的 Gatan Alpine 探测器。与 Gatan K3 相比,Alpine 在这些电压下的 DQE 有了显著提高,特别是在 100 keV 下的 Nyquist 值提高了 4 倍。在单颗粒低温电子显微镜实验中,Alpine 数据集在配备非标准 SP-Twin 镜头的 ThermoFisher Scientific (TFS) Glacios 显微镜上,在 120 和 200 keV 电压下重建了分辨率优于 2 Å 的去铁蛋白。我们还对 115 kDa 不对称蛋白质复合物进行了分辨率为 ∼ 3.2 Å 的重建,证明了其在复杂生物样本中的有效性。深入的分析表明,阿尔卑斯重建与 K3 在 200 keV 时的重建结果相当,而且值得注意的是,阿尔卑斯重建在 TFS Glacios 上 120 keV 时的结果超过了所有其他数据,只有在 TFS Titan Krios 上使用 GIF/K3 重建的 300 keV 数据除外。此外,我们还展示了 Alpine 在较低端系统上进行高分辨率数据采集和筛选的能力,在 100 keV 下获得了分辨率为 3 Å 的apoferritin 和 aldolase 重建,并使用侧入式低温支架获得了 55 kDa 样品的详细二维平均值。总之,我们的研究表明,Gatan Alpine 在标准 200 keV 成像系统中表现出色,并有可能捕捉到较低加速电压的好处,从而有可能将较小尺寸的粒子纳入低温电子显微镜的范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-resolution single-particle imaging at 100–200 keV with the Gatan Alpine direct electron detector

High-resolution single-particle imaging at 100–200 keV with the Gatan Alpine direct electron detector

Developments in direct electron detector technology have played a pivotal role in enabling high-resolution structural studies by cryo-EM at 200 and 300 keV. Yet, theory and recent experiments indicate advantages to imaging at 100 keV, energies for which the current detectors have not been optimized. In this study, we evaluated the Gatan Alpine detector, designed for operation at 100 and 200 keV. Compared to the Gatan K3, Alpine demonstrated a significant DQE improvement at these energies, specifically a ∼ 4-fold improvement at Nyquist at 100 keV. In single-particle cryo-EM experiments, Alpine datasets yielded better than 2 Å resolution reconstructions of apoferritin at 120 and 200 keV on a ThermoFisher Scientific (TFS) Glacios microscope fitted with a non-standard SP-Twin lens. We also achieved a ∼ 3.2 Å resolution reconstruction of a 115 kDa asymmetric protein complex, proving Alpine's effectiveness with complex biological samples. In-depth analysis revealed that Alpine reconstructions are comparable to K3 reconstructions at 200 keV, and remarkably, reconstruction from Alpine at 120 keV on a TFS Glacios surpassed all but the 300 keV data from a TFS Titan Krios with GIF/K3. Additionally, we show Alpine’s capability for high-resolution data acquisition and screening on lower-end systems by obtaining ∼ 3 Å resolution reconstructions of apoferritin and aldolase at 100 keV and detailed 2D averages of a 55 kDa sample using a side-entry cryo holder. Overall, we show that Gatan Alpine performs well with the standard 200 keV imaging systems and may potentially capture the benefits of lower accelerating voltages, bringing smaller sized particles within the scope of cryo-EM.

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来源期刊
Journal of structural biology
Journal of structural biology 生物-生化与分子生物学
CiteScore
6.30
自引率
3.30%
发文量
88
审稿时长
65 days
期刊介绍: Journal of Structural Biology (JSB) has an open access mirror journal, the Journal of Structural Biology: X (JSBX), sharing the same aims and scope, editorial team, submission system and rigorous peer review. Since both journals share the same editorial system, you may submit your manuscript via either journal homepage. You will be prompted during submission (and revision) to choose in which to publish your article. The editors and reviewers are not aware of the choice you made until the article has been published online. JSB and JSBX publish papers dealing with the structural analysis of living material at every level of organization by all methods that lead to an understanding of biological function in terms of molecular and supermolecular structure. Techniques covered include: • Light microscopy including confocal microscopy • All types of electron microscopy • X-ray diffraction • Nuclear magnetic resonance • Scanning force microscopy, scanning probe microscopy, and tunneling microscopy • Digital image processing • Computational insights into structure
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