Radiation-dose effects in correlative X-ray/cryo-electron microscopy of frozen-hydrated biological samples.

IF 4.3 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Thorsten B Blum, Vincent Olieric, Ana Diaz, Takashi Ishikawa, Volodymyr M Korkhov
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Abstract

In cryo-electron microscopy (cryo-EM), imaging of biological specimens is restricted by the limited field of view and by sample thickness. Hard X-ray imaging, with its ability to penetrate samples several tens of micrometres thick, offers a complementary approach for high-resolution visualization. A major concern is whether cryo-preserved samples can withstand the handling conditions at synchrotron facilities without excessive icing, and whether the radiation exposure during X-ray imaging compromises specimen integrity, thereby hindering subsequent attempts to achieve high-resolution 3D reconstructions via cryo-EM. To evaluate this, we deposited apoferritin samples on a cryo-EM grid, exposed them to varied X-ray doses typical for X-ray tomography experiments at a synchrotron facility, and subsequently analysed the exposed particles by cryo-EM. Despite the apparent damage sustained throughout the experiment, the samples remained amenable to cryo-EM analysis, with structural details at a resolution of ∼4 Å at the highest absorbed X-ray dose of 100 MGy. By comparison, a similar cryo-EM dataset of apoferritin particles that were not exposed to X-rays but were mounted on the same cryo-EM grid resulted in a 3D reconstruction at 3.17 Å resolution. Thus, while radiation damage may limit the high-resolution information in specimens processed by cryo-X-ray tomography, the cryo-preserved biological material exposed to these high X-ray doses can still be used for subsequent cryo-EM workflows aiming to obtain structural biology insights at intermediate to high resolution. These findings lay the groundwork for an integrated imaging workflow that combines X-ray and cryo-EM techniques to enable multiscale analysis of thick vitrified biological specimens.

冷冻水合生物样品的相关x射线/冷冻电镜辐射剂量效应。
在低温电子显微镜(cryo-EM)中,生物标本的成像受到有限视野和样品厚度的限制。硬x射线成像能够穿透几十微米厚的样品,为高分辨率可视化提供了一种补充方法。一个主要的问题是,冷冻保存的样品是否能够承受同步加速器设施的处理条件而不过度结冰,以及x射线成像期间的辐射暴露是否会损害样品的完整性,从而阻碍后续通过冷冻电镜实现高分辨率3D重建的尝试。为了评估这一点,我们将载铁蛋白样品沉积在冷冻电镜网格上,将它们暴露在同步加速器设施中x射线断层扫描实验中典型的不同x射线剂量下,随后通过冷冻电镜分析暴露的颗粒。尽管在整个实验过程中存在明显的损伤,但样品仍然可以进行冷冻电镜分析,在最高吸收x射线剂量为100 MGy时,结构细节的分辨率为~ 4 Å。相比之下,类似的铁蛋白颗粒的低温电镜数据集没有暴露在x射线下,但安装在相同的低温电镜网格上,以3.17 Å分辨率进行了三维重建。因此,虽然辐射损伤可能会限制冷冻x射线断层扫描处理标本的高分辨率信息,但暴露于这些高x射线剂量的冷冻保存生物材料仍然可以用于后续的冷冻em工作流程,旨在获得中至高分辨率的结构生物学见解。这些发现为集成成像工作流程奠定了基础,该流程结合了x射线和冷冻电镜技术,可以对厚玻璃化生物标本进行多尺度分析。
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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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