ExoSloNano: multimodal nanogold labels for identification of macromolecules in live cells and cryo-electron tomograms

In situ cryo-electron microscopy (cryo-EM) enables the direct interrogation of structure-function relationships by resolving macromolecular structures in their native cellular environment. Recent progress in sample preparation, imaging and data processing has enabled the identification and determination of large biomolecular complexes. However, the majority of proteins are of a size that still eludes identification in cellular cryo-EM data, and most proteins exist in low copy numbers. Therefore, novel tools are needed for cryo-EM to identify macromolecules across multiple size scales (from microns to nanometers). Here we introduce nanogold probes for detecting specific proteins using correlative light and electron microscopy, cryo-electron tomography (cryo-ET) and resin-embedded electron microscopy. These nanogold probes can be introduced into live cells, in a manner that preserves intact molecular networks and cell viability. We use this ExoSloNano system to identify both cytoplasmic and nuclear proteins by room-temperature electron microscopy, and resolve associated structures by cryo-ET. By providing high-efficiency protein labeling in live cells and molecular specificity within cryo-ET tomograms, ExoSloNano expands the proteome available to electron microscopy.

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Publication Details

Journal
Nature Methods
Published
2025-11-28
DOI
https://doi.org/10.1038/s41592-025-02928-4
Citations
1
Primary Topic
Advanced Electron Microscopy Techniques and Applications
Type
article
Field-Weighted Citation Impact
2.55
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article

ExoSloNano: multimodal nanogold labels for identification of macromolecules in live cells and cryo-electron tomograms

Alice Sherrard, Joshua Hutchings, Michael K. Rosen, Lindsey N. Young et al.
1 citations
Nature Methods
Advanced Electron Microscopy Techniques and Applications
2.55
article

ExoSloNano: multimodal nanogold labels for identification of macromolecules in live cells and cryo-electron tomograms

Alice Sherrard, Joshua Hutchings, Michael K. Rosen, Lindsey N. Young, Huabin Zhou, Margot Riggi, Antonio J. Giráldez, Farhaz Shaikh, Elizabeth Villa, Eric J. Bennett, Meena L. Narasimhan, W. Alexander Flaherty
article en
1 citations

Abstract

In situ cryo-electron microscopy (cryo-EM) enables the direct interrogation of structure-function relationships by resolving macromolecular structures in their native cellular environment. Recent progress in sample preparation, imaging and data processing has enabled the identification and determination of large biomolecular complexes. However, the majority of proteins are of a size that still eludes identification in cellular cryo-EM data, and most proteins exist in low copy numbers. Therefore, novel tools are needed for cryo-EM to identify macromolecules across multiple size scales (from microns to nanometers). Here we introduce nanogold probes for detecting specific proteins using correlative light and electron microscopy, cryo-electron tomography (cryo-ET) and resin-embedded electron microscopy. These nanogold probes can be introduced into live cells, in a manner that preserves intact molecular networks and cell viability. We use this ExoSloNano system to identify both cytoplasmic and nuclear proteins by room-temperature electron microscopy, and resolve associated structures by cryo-ET. By providing high-efficiency protein labeling in live cells and molecular specificity within cryo-ET tomograms, ExoSloNano expands the proteome available to electron microscopy.

Nature MethodsVol. 23(1)
Howard Hughes Medical Institute (US), University of California, San Francisco (US), Yale Cancer Center (US), Yale University (US), University of California San Diego (US), Chan Zuckerberg Initiative (United States) (US), Max Planck Institute of Biochemistry (DE), The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 8%
Advanced Electron Microscopy Techniques and Applications
2.55
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