Pillar data-acquisition strategies for cryo-electron tomography of beam-sensitive biological samples.

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
James M Parkhurst, Trond Varslot, Maud Dumoux, C Alistair Siebert, Michele Darrow, Mark Basham, Angus Kirkland, Michael Grange, Gwyndaf Evans, James H Naismith
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引用次数: 0

Abstract

For cryo-electron tomography (cryo-ET) of beam-sensitive biological specimens, a planar sample geometry is typically used. As the sample is tilted, the effective thickness of the sample along the direction of the electron beam increases and the signal-to-noise ratio concomitantly decreases, limiting the transfer of information at high tilt angles. In addition, the tilt range where data can be collected is limited by a combination of various sample-environment constraints, including the limited space in the objective lens pole piece and the possible use of fixed conductive braids to cool the specimen. Consequently, most tilt series are limited to a maximum of ±70°, leading to the presence of a missing wedge in Fourier space. The acquisition of cryo-ET data without a missing wedge, for example using a cylindrical sample geometry, is hence attractive for volumetric analysis of low-symmetry structures such as organelles or vesicles, lysis events, pore formation or filaments for which the missing information cannot be compensated by averaging techniques. Irrespective of the geometry, electron-beam damage to the specimen is an issue and the first images acquired will transfer more high-resolution information than those acquired last. There is also an inherent trade-off between higher sampling in Fourier space and avoiding beam damage to the sample. Finally, the necessity of using a sufficient electron fluence to align the tilt images means that this fluence needs to be fractionated across a small number of images; therefore, the order of data acquisition is also a factor to consider. Here, an n-helix tilt scheme is described and simulated which uses overlapping and interleaved tilt series to maximize the use of a pillar geometry, allowing the entire pillar volume to be reconstructed as a single unit. Three related tilt schemes are also evaluated that extend the continuous and classic dose-symmetric tilt schemes for cryo-ET to pillar samples to enable the collection of isotropic information across all spatial frequencies. A fourfold dose-symmetric scheme is proposed which provides a practical compromise between uniform information transfer and complexity of data acquisition.

用于对光束敏感的生物样品进行低温电子断层扫描的柱状数据采集策略。
在对电子束敏感的生物样本进行低温电子断层成像(cryo-ET)时,通常使用平面样本几何形状。随着样本的倾斜,样本沿电子束方向的有效厚度增加,信噪比随之降低,从而限制了高倾斜角度下的信息传输。此外,可采集数据的倾斜范围还受到各种样品环境限制的综合影响,包括物镜极片的有限空间和使用固定导电编织物冷却试样的可能性。因此,大多数倾斜系列的最大值都限制在 ±70°,导致傅立叶空间中出现一个缺失的楔形。因此,对于细胞器或囊泡、裂解事件、孔隙形成或丝状物等低对称性结构的容积分析而言,获取无缺失楔形的低温电子显微镜数据(例如使用圆柱形样品几何结构)是非常有吸引力的,因为平均技术无法弥补缺失的信息。无论采用哪种几何结构,电子束对试样的损伤都是一个问题,而且最先获得的图像将比最后获得的图像传递更多的高分辨率信息。在傅立叶空间的高采样率和避免电子束对样品的损伤之间也存在固有的权衡问题。最后,由于必须使用足够的电子通量来对齐倾斜图像,这就意味着需要在少量图像中分散电子通量;因此,数据采集的顺序也是一个需要考虑的因素。这里描述并模拟了一种 n 螺旋倾斜方案,该方案使用重叠和交错的倾斜序列来最大限度地利用支柱几何形状,从而将整个支柱体积作为一个单元进行重建。此外,还评估了三种相关的倾斜方案,它们将用于低温电子显微镜的连续和经典剂量对称倾斜方案扩展到了柱状样本,从而能够收集所有空间频率的各向同性信息。提出的四倍剂量对称方案在均匀信息传输和数据采集复杂性之间提供了实用的折中方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Crystallographica. Section D, Structural Biology
Acta Crystallographica. Section D, Structural Biology BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
4.50
自引率
13.60%
发文量
216
期刊介绍: Acta Crystallographica Section D welcomes the submission of articles covering any aspect of structural biology, with a particular emphasis on the structures of biological macromolecules or the methods used to determine them. Reports on new structures of biological importance may address the smallest macromolecules to the largest complex molecular machines. These structures may have been determined using any structural biology technique including crystallography, NMR, cryoEM and/or other techniques. The key criterion is that such articles must present significant new insights into biological, chemical or medical sciences. The inclusion of complementary data that support the conclusions drawn from the structural studies (such as binding studies, mass spectrometry, enzyme assays, or analysis of mutants or other modified forms of biological macromolecule) is encouraged. Methods articles may include new approaches to any aspect of biological structure determination or structure analysis but will only be accepted where they focus on new methods that are demonstrated to be of general applicability and importance to structural biology. Articles describing particularly difficult problems in structural biology are also welcomed, if the analysis would provide useful insights to others facing similar problems.
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