A cryogenic, coincident fluorescence, electron and ion beam microscope

Boltje, D.; Hoogenboom, J.; Jakobi, A. J.; Jensen, G. J.; Jonker, C.; Kaag, M.; Koster, A. J.; Last, M.; de Agrela Pinto, C.; Plitzko, J. M.; Raunser, S.; Tacke, S.; Wang, Z.; van der Wee, E.; Wepf, R.; den Hoedt, S.

doi:10.1101/2022.09.02.506334

bioRxiv · 10.1101/2022.09.02.506334

A cryogenic, coincident fluorescence, electron and ion beam microscope

Boltje, D.·Hoogenboom, J.·Jakobi, A. J.·Jensen, G. J.·Jonker, C.·Kaag, M.·Koster, A. J.·Last, M.·de Agrela Pinto, C.·Plitzko, J. M.·Raunser, S.·Tacke, S.·Wang, Z.·van der Wee, E.·Wepf, R.·den Hoedt, S.

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Abstract

Cryogenic electron tomography (cryo-ET) combined with sub-tomogram averaging, allows in-situ visualisation and structure determination of macromolecular complexes at sub-nanometre resolution. Cryogenic focused ion beam (cryo-FIB) micromachining is used to prepare a thin lamella-shaped sample out of a frozen-hydrated cell for cryo-ET imaging, but standard cryo-FIB fabrication is blind to the precise location of the structure or proteins of interest. Fluorescence-guided focused ion beam (FIB) milling at target locations requires multiple sample transfers prone to contamination, and relocation and registration accuracy is often insufficient for 3D targeting. Here, we present in-situ fluoresence microscopy-guided FIB fabrication of a frozen-hydrated lamella to solve this problem: we built a coincident 3-beam cryogenic correlative microscope by retrofitting a compact cryogenic microcooler, custom positioning stage, and an inverted widefield fluorescence microscope (FM) on an existing focused ion-beam scanning electron microscope (FIB-SEM). We show FM controlled targeting at every milling step in the lamella fabrication process, validated with transmission electron microscope (TEM) tomogram reconstructions of the target regions. The ability to check the lamella during and after the milling process results in a higher success rate in the fabrication process and will increase the throughput of fabrication for lamellae suitable for high-resolution imaging.

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Boltje, D., Hoogenboom, J., Jakobi, A. J., Jensen, G. J., Jonker, C., Kaag, M., Koster, A. J., Last, M., de Agrela Pinto, C., Plitzko, J. M., Raunser, S., Tacke, S., Wang, Z., van der Wee, E., Wepf, R., den Hoedt, S.. 2022-09-03. A cryogenic, coincident fluorescence, electron and ion beam microscope. https://doi.org/10.1101/2022.09.02.506334

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