Department of Mechanical Engineering and Materials Science, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA.
J Microsc. 2012 Sep;247(3):220-7. doi: 10.1111/j.1365-2818.2012.03635.x.
Focused ion beam milling at cryogenic temperatures (cryo-FIB) is a valuable tool that can be used to thin vitreous biological specimens for subsequent imaging and analysis by cryo-transmission electron microscopy (cryo-TEM) in a frozen-hydrated state. This technique offers the potential benefit of eliminating the mechanical artefacts that are typically found with cryo-ultramicrotomy. However, due to the additional complexity in transferring samples in and out of the FIB, contamination and devitrification of the amorphous ice is commonly encountered. To address these problems, we have designed a sample cryo-shuttle that directly and specifically accepts Polara TEM cartridges to simplify the transfer process between FIB and TEM. We optimized several parameters in the cryo-FIB and cryo-TEM processes using the quality of the samples' ice as an indicator and demonstrated high-quality milling with large mammalian cells. By comparing the results from HeLa cells to those from Escherichia coli cells, we discuss some of the artefacts and challenges we have encountered using this technique.
低温聚焦离子束铣削(cryo-FIB)是一种非常有价值的工具,可用于对玻璃态生物样本进行减薄,以便在冷冻水合状态下通过低温透射电子显微镜(cryo-TEM)进行后续成像和分析。该技术具有消除通常在低温超薄切片中发现的机械伪影的潜在优势。然而,由于在 FIB 中进出样品的额外复杂性,经常会遇到污染和无定形冰的失玻璃化。为了解决这些问题,我们设计了一种样品低温梭子,它可以直接且专门接受 Polara TEM 盒,以简化 FIB 和 TEM 之间的转移过程。我们使用样品冰的质量作为指标,对低温 FIB 和低温 TEM 过程中的几个参数进行了优化,并使用大型哺乳动物细胞进行了高质量的铣削。通过将 HeLa 细胞的结果与大肠杆菌细胞的结果进行比较,我们讨论了使用该技术时遇到的一些伪影和挑战。