Cryogenic focused ion beam (FIB) milling is essential for fabricating thin lamella-shaped samples out of frozen-hydrated cells for high-resolution structure determination. Structural information can only be resolved at high resolution if the lamella thickness is between 100 and 200Â nm. While the lamella fabrication workflow has improved significantly since its conception, quantitative, live feedback on lamella thickness, quality, and biological target inclusion remains lacking. Using coincident light microscopy integrated into the FIB scanning electron microscope (FIB-SEM), we present three strategies that enable accurate, live control during lamella fabrication. First, we combine four-dimensional (4D) STEM with fluorescence microscopy (FM) targeting to determine lamella thickness. Second, with reflected light microscopy (RLM), we screen target sites for ice contamination and monitor lamella thickness and protective Pt coating integrity during FIB milling. Third, we exploit thin-film interference for fine-grained feedback on thickness uniformity below 500Â nm. Finally, we present a fluorescence-targeted, quality-controlled workflow for frozen-hydrated lamellae, benchmarked with excellent agreement with energy-filtered transmission electron microscopy (EFTEM) measurements and tomograms from electron cryotomography.
Thickness- and quality-controlled fabrication of fluorescence-targeted frozen-hydrated lamellae.
厚度和质量可控的荧光靶向冷冻水合薄片的制备
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作者:Boltje Daan B, Skoupý Radim, Taisne Clémence, Evers Wiel H, Jakobi Arjen J, Hoogenboom Jacob P
| 期刊: | Cell Reports Methods | 影响因子: | 4.500 |
| 时间: | 2025 | 起止号: | 2025 Mar 24; 5(3):101004 |
| doi: | 10.1016/j.crmeth.2025.101004 | ||
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