Microtubules as a versatile reference standard for expansion microscopy

Expansion microscopy (ExM) is continually improving, and new ExM variants need to be validated on well-defined biological structures. There is no consensus on validation structures for ExM, especially as nuclear pore complexes or DNA nanorulers are not popular for ExM studies. Here we propose that microtubules should be used for ExM validation. The diameter of microtubules immunostained using primary and secondary antibodies is sufficiently large for the validation of techniques with resolutions better than 50 nm. For techniques with higher precision (up to ~10 nm), microtubules can be assembled and imaged in vitro, using a protocol that we introduce here. Alternatively, a cellular extraction procedure can be employed, followed by labeling the peptide chains of the tubulin molecules with NHS-ester fluorophores. Finally, for nanometer-scale techniques, single tubulin molecules can be analyzed. We conclude that microtubules are valuable structures for the validation of ExM and related technologies.

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Publication Details

Journal
Communications Biology
Published
2025-03-26
DOI
https://doi.org/10.1038/s42003-025-07967-3
Citations
4
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
6.54

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article

Microtubules as a versatile reference standard for expansion microscopy

Rajdeep Chowdhury, Tiago Mimoso, Sarah Köster, Silvio O. Rizzoli et al.
4 citations
Communications Biology
Advanced Fluorescence Microscopy Techniques
6.54
article

Microtubules as a versatile reference standard for expansion microscopy

Rajdeep Chowdhury, Tiago Mimoso, Sarah Köster, Silvio O. Rizzoli, Donatus Krah, Abed Alrahman Chouaib, Nikolaos Mougios, Felipe Opazo, Ali H. Shaib
article en
4 citations

Abstract

Expansion microscopy (ExM) is continually improving, and new ExM variants need to be validated on well-defined biological structures. There is no consensus on validation structures for ExM, especially as nuclear pore complexes or DNA nanorulers are not popular for ExM studies. Here we propose that microtubules should be used for ExM validation. The diameter of microtubules immunostained using primary and secondary antibodies is sufficiently large for the validation of techniques with resolutions better than 50 nm. For techniques with higher precision (up to ~10 nm), microtubules can be assembled and imaged in vitro, using a protocol that we introduce here. Alternatively, a cellular extraction procedure can be employed, followed by labeling the peptide chains of the tubulin molecules with NHS-ester fluorophores. Finally, for nanometer-scale techniques, single tubulin molecules can be analyzed. We conclude that microtubules are valuable structures for the validation of ExM and related technologies.

Communications BiologyVol. 8(1)
Universitätsmedizin Göttingen (DE), Nanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103 (DE), Verbundzentrale des GBV (DE), University of Göttingen (DE), GITAM University (IN), Saarland University (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 4%
Advanced Fluorescence Microscopy Techniques
6.54
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Microtubules as a versatile reference standard for expansion microscopy — Rajdeep Chowdhury, Tiago Mimoso, et al. · Communications Biology (2025) | TGRS Research Map | TGRS