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Effects of base temperature, immersion medium, and EM grid material on devitrification thresholds in cryogenic optical super-resolution microscopy

  • Soheil Mojiri
  • , Joseph M. Dobbs
  • , Niko Faul
  • , Thomas P. Burg
  • , Julia Mahamid
  • , Jonas Ries

Veröffentlichungen: Beitrag in FachzeitschriftArtikelPeer Reviewed

Abstract

Cryogenic correlative light and electron microscopy (cryo-CLEM) is an imaging strategy that integrates specific molecular labeling and molecular resolution structural information. However, there is a resolution gap of more than two orders of magnitude between diffraction-limited fluorescence microscopy and electron microscopy (EM). Single-molecule localization microscopy (SMLM) performed at cryogenic temperatures promises to bridge this resolution gap. Nevertheless, the high excitation laser powers required for SMLM risk the devitrification of frozen biological samples, leading to perturbation of their native-like state. Here, we investigate how base cooling temperature, immersion medium, and EM grid support materials influence sample devitrification. Using finite element simulations and experimental validation, we show that a cryo-immersion medium enhances heat dissipation for carbon supports, while metallic supports in a cold nitrogen gas medium tolerate higher laser intensities due to lower base temperatures. Gold supports illuminated at 640nm exhibit markedly high laser thresholds, similar to silver-coated grids. Additionally, metallic supports maintain efficient heat dissipation in vacuum-based cryostats. Our findings provide quantitative insights that aid in optimization of cryo-SMLM setups for improved cryo-CLEM imaging.

OriginalspracheEnglisch
Aufsatznummer108231
FachzeitschriftJournal of Structural Biology
Jahrgang217
Ausgabenummer3
DOIs
PublikationsstatusVeröffentlicht - Sept. 2025

Fördermittel

This work was supported by the Chan Zuckerberg Initiative (CZI) Visual Proteomics Program (Grant No. 2021 – 234620 ), the EMBL , and the European Research Council under the European Union’s Horizon 2020 Research and Innovation Program (Grant No. 772441 ). The authors acknowledge the facilities provided by the EMBL Cryo-EM Platform and the EMBL Imaging Centre, the support of Harald Hess, Gleb Shtengel, and James Seyforth at the Janelia Research Campus for their guidance and assistance in conducting the dosing experiments with the vacuum cryostat microscope, and the cryo-electron microscopy facility team at Janelia, especially Zhiheng Yu, Momoko Shiozaki, and Xiaowei Zhao, for their help during imaging. Finally, we thank the group members of J.M., J.R., and T.P.B. for their insightful discussions and valuable input throughout this work.

ÖFOS 2012

  • 106041 Strukturbiologie

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