Correlative Light and Electron Cryo-Microscopy Workflow Combining Micropatterning, Ice Shield, and an In-Chamber Fluorescence Light Microscope
Sabrina Berkamp,
Deniz Daviran,
Marit Smeets,
Alexane Caignard,
Riddhi Jani,
Pia Sundermeyer,
Caspar Jonker,
Sven Gerlach,
Bernd Hoffmann,
Katherine Lau,
Carsten Sachse
Affiliations
Sabrina Berkamp
Ernst-Ruska Centre for Microscopy and Spectroscopy with Electrons, ER-C-3/Structural Biology, Forschungszentrum Jülich, Jülich, GermanyInstitute of Biological Information Processing, IBI-6: Structural Cell Biology, Forschungszentrum Jülich, Jülich, Germany
Deniz Daviran
Delmic BV, Delft, the Netherlands
Marit Smeets
Delmic BV, Delft, the Netherlands
Alexane Caignard
Alvéole, Paris, France
Riddhi Jani
Alvéole, Paris, France
Pia Sundermeyer
Ernst-Ruska Centre for Microscopy and Spectroscopy with Electrons, ER-C-3/Structural Biology, Forschungszentrum Jülich, Jülich, GermanyInstitute of Biological Information Processing, IBI-6: Structural Cell Biology, Forschungszentrum Jülich, Jülich, Germany
Caspar Jonker
Delmic BV, Delft, the Netherlands
Sven Gerlach
Institute of Biological Information Processing, IBI-2: Mechanobiology Forschungszentrum Jülich, Jülich, Germany
Bernd Hoffmann
Institute of Biological Information Processing, IBI-2: Mechanobiology Forschungszentrum Jülich, Jülich, Germany
Katherine Lau
Delmic BV, Delft, the Netherlands
Carsten Sachse
Ernst-Ruska Centre for Microscopy and Spectroscopy with Electrons, ER-C-3/Structural Biology, Forschungszentrum Jülich, Jülich, GermanyInstitute of Biological Information Processing, IBI-6: Structural Cell Biology, Forschungszentrum Jülich, Jülich, Germany, Department of Biology, Heinrich Heine University, Düsseldorf, Germany
In situ cryo-electron tomography (cryo-ET) is the most current, state-of-the-art technique to study cell machinery in its hydrated near-native state. The method provides ultrastructural details at sub-nanometer resolution for many components within the cellular context. Making use of recent advances in sample preparation techniques and combining this method with correlative light and electron microscopy (CLEM) approaches have enabled targeted molecular visualization. Nevertheless, the implementation has also added to the complexity of the workflow and introduced new obstacles in the way of streamlining and achieving high throughput, sample yield, and sample quality. Here, we report a detailed protocol by combining multiple newly available technologies to establish an integrated, high-throughput, optimized, and streamlined cryo-CLEM workflow for improved sample yield.Key features• PRIMO micropatterning allows precise cell positioning and maximum number of cell targets amenable to thinning with cryo focused-ion-beam–scanning electron microscopy.• CERES ice shield ensures that the lamellae remain free of ice contamination during the batch milling process.• METEOR in-chamber fluorescence microscope facilitates the targeted cryo focused-ion-beam (cryo FIB) milling of these targets.• Combining the three technologies into one cryo-CLEM workflow maximizes sample yield, throughput, and efficiency.Graphical overview