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蜂巢金标本支持实现对拉长细胞的正交聚焦离子束铣削,以进行冷冻电镜术。

Honeycomb gold specimen supports enabling orthogonal focussed ion beam-milling of elongated cells for cryo-ET.

机构信息

MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.

MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.

出版信息

J Struct Biol. 2024 Jun;216(2):108097. doi: 10.1016/j.jsb.2024.108097. Epub 2024 May 19.

DOI:10.1016/j.jsb.2024.108097
PMID:38772448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7616276/
Abstract

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.

摘要

冷冻聚焦离子束(FIB)-铣削是一种强大的技术,通过电子冷冻断层扫描(cryo-ET)可以将厚的、细胞状的样本开放到高分辨率的结构分析中。FIB 铣削的薄片可以从网格上的细胞中产生,也可以从较厚的、高压冷冻的样本中切割。然而,这些方法可能会对样本施加几何约束,这可能是无益的,特别是在对具有非常确定取向的细胞内结构进行成像时。例如, plunge 冷冻的棒状细菌与网格平面平行取向,然而,Z 环,一种类似于微管蛋白的 FtsZ 纤维状结构,是细菌分裂的关键组织者,它环绕细胞的周长延伸,因此与成像平面垂直。因此,用当前的技术很难或不可能对许多完整的环进行成像。为了克服这个问题,我们制造了具有蜂窝状几何形状的规则圆柱形孔阵列的整体金制样本支架,将细菌固定在垂直方向。这些支架,我们称之为“蜂窝金盘”,替代了标准的 EM 网格,并且与 FIB 铣削结合使用,可以生产出包含细胞横截面的薄片。所得的薄片比传统的薄片更稳定,不易断裂和充电。蜂窝盘的设计可以根据需要进行修改,因此也将能够对其他在难以获得的取向中进行 cryo-ET 和 cryo-EM 成像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/97dc298f14cf/EMS197563-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/5cc2c1dd6f55/EMS197563-f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/05033aeb5cd3/EMS197563-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/68c69b753f6c/EMS197563-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/b0a54d78db5c/EMS197563-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/cbe899cd29b3/EMS197563-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/a810f58517e5/EMS197563-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/97dc298f14cf/EMS197563-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/5cc2c1dd6f55/EMS197563-f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/05033aeb5cd3/EMS197563-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/68c69b753f6c/EMS197563-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/b0a54d78db5c/EMS197563-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/cbe899cd29b3/EMS197563-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/a810f58517e5/EMS197563-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bf9/7616276/97dc298f14cf/EMS197563-f006.jpg

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本文引用的文献

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