Victoria L. Hale, James Hooker, Christopher J. Russo, Jan Löwe
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It is therefore difficult or impractical to image many complete rings with current technologies. To circumvent this problem, we have fabricated monolithic gold specimen supports with a regular array of cylindrical wells in a honeycomb geometry, which trap bacteria in a vertical orientation. These supports, which we call “honeycomb gold discs”, replace standard EM grids and when combined with FIB-milling enable the production of lamellae containing cross-sections through cells. The resulting lamellae are more stable and resistant to breakage and charging than conventional lamellae. 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引用次数: 0
摘要
低温聚焦离子束(FIB)铣削技术是一项强大的技术,可通过电子冷冻电镜技术(cryo-ET)对较厚的细胞标本进行高分辨率结构分析。FIB 研磨薄片可以从网格上的细胞中产生,也可以从较厚的高压冷冻标本中切割。然而,这些方法可能会对试样造成几何限制,尤其是在对细胞内方向非常明确的结构进行成像时,这些限制可能无济于事。例如,冷冻棒状细菌的方向与网格平面平行,但 Z 环(一种由管状蛋白 FtsZ 组成的丝状结构,是细菌分裂的关键组织者)围绕细胞的圆周运行,与成像平面垂直。因此,利用现有技术对许多完整的环进行成像非常困难或不切实际。为了解决这个问题,我们制作了整体式金试样支架,支架上有蜂窝状几何形状的规则圆柱形孔阵列,能以垂直方向捕获细菌。我们称这些支撑物为 "蜂巢金盘",它们可以取代标准的电磁网格,与 FIB 研磨技术相结合,可以制作出包含细胞横截面的薄片。与传统薄片相比,这种薄片更稳定、更耐破损和充电。蜂窝状圆盘的设计可根据需要进行修改,因此还能在其他难以获得的方向对其他标本进行低温电子显微镜和低温电磁成像。
Honeycomb gold specimen supports enabling orthogonal focussed ion beam-milling of elongated cells for cryo-ET
Cryo-focussed ion beam (FIB)-milling is a powerful technique that opens up thick, cellular specimens to high-resolution structural analysis by electron cryotomography (cryo-ET). FIB-milled lamellae can be produced from cells on grids, or cut from thicker, high-pressure frozen specimens. However, these approaches can put geometrical constraints on the specimen that may be unhelpful, particularly when imaging structures within the cell that have a very defined orientation. For example, plunge frozen rod-shaped bacteria orient parallel to the plane of the grid, yet the Z-ring, a filamentous structure of the tubulin-like protein FtsZ and the key organiser of bacterial division, runs around the circumference of the cell such that it is perpendicular to the imaging plane. It is therefore difficult or impractical to image many complete rings with current technologies. To circumvent this problem, we have fabricated monolithic gold specimen supports with a regular array of cylindrical wells in a honeycomb geometry, which trap bacteria in a vertical orientation. These supports, which we call “honeycomb gold discs”, replace standard EM grids and when combined with FIB-milling enable the production of lamellae containing cross-sections through cells. The resulting lamellae are more stable and resistant to breakage and charging than conventional lamellae. The design of the honeycomb discs can be modified according to need and so will also enable cryo-ET and cryo-EM imaging of other specimens in otherwise difficult to obtain orientations.
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