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Cryogenic electron tomography by the numbers: Charting underexplored lineages in structural cell biology.

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Bibliographic Details
Title: Cryogenic electron tomography by the numbers: Charting underexplored lineages in structural cell biology.
Authors: Ansell, T. Bertie1,2 bansell5@stanford.edu, Berrios, Louis1,3, Peay, Kabir G.1,4, Dahlberg, Peter D.2
Source: Proceedings of the National Academy of Sciences of the United States of America. 2/24/2026, Vol. 123 Issue 8, p1-9. 45p.
Subjects: Electron microscope techniques, Biodiversity, Multicellular organisms, Electron microscopy, Phylogeny, Cell anatomy, High resolution imaging
Abstract: Imaging cells and their interactions across the whole biosphere with molecular-scale resolution is key for understanding structure-function relations. Cryogenic electron tomography (cryo-ET) is a powerful method for obtaining this critical information. However, cryo-ET studies are challenging and often limited to a small number of cell types per study. Here, we collate cryo-ET data from hundreds of cells and tissues across the biosphere to i) identify emerging methodological trends, ii) pinpoint strategies to reduce imaging time and costs, iii) quantitatively compare methods for cell freezing and sectioning, and iv) census cryo-ET species coverage across all domains of life. Comparing the fraction of cellular material within a single lamella across all domains of life reveals an order of magnitude difference between eukaryotes (1%) compared to bacteria (9%) and archaea (14%). We calculate the fraction of cellular material which can be imaged using distinct sectioning methods on multicellular communities and tissues--identifying serial lift-out as a powerful approach for obtaining more complete cellular depictions. Finally, we show that the biodiversity of current cryo-ET studies is 2 to 3 orders of magnitude lower than in sequence libraries and 4 to 5 lower than the total predicted on Earth. Our analyses reveal major evolutionary lineages which remain critically understudied and highlight where future cryo-ET research would be most impactful. [ABSTRACT FROM AUTHOR]
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Database: Engineering Source
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Abstract:Imaging cells and their interactions across the whole biosphere with molecular-scale resolution is key for understanding structure-function relations. Cryogenic electron tomography (cryo-ET) is a powerful method for obtaining this critical information. However, cryo-ET studies are challenging and often limited to a small number of cell types per study. Here, we collate cryo-ET data from hundreds of cells and tissues across the biosphere to i) identify emerging methodological trends, ii) pinpoint strategies to reduce imaging time and costs, iii) quantitatively compare methods for cell freezing and sectioning, and iv) census cryo-ET species coverage across all domains of life. Comparing the fraction of cellular material within a single lamella across all domains of life reveals an order of magnitude difference between eukaryotes (1%) compared to bacteria (9%) and archaea (14%). We calculate the fraction of cellular material which can be imaged using distinct sectioning methods on multicellular communities and tissues--identifying serial lift-out as a powerful approach for obtaining more complete cellular depictions. Finally, we show that the biodiversity of current cryo-ET studies is 2 to 3 orders of magnitude lower than in sequence libraries and 4 to 5 lower than the total predicted on Earth. Our analyses reveal major evolutionary lineages which remain critically understudied and highlight where future cryo-ET research would be most impactful. [ABSTRACT FROM AUTHOR]
ISSN:00278424
DOI:10.1073/pnas.2518350123