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GelMap: Intrinsic calibration and deformation mapping for expansion microscopy

Hugo G.J. Damstra, Josiah B. Passmore, Albert K. Serweta, Ioannis Koutlas, Mithila Burute, Frank J. Meye, Anna Akhmanova, Lukas C. Kapitein
doi: https://doi.org/10.1101/2022.12.21.521394
Hugo G.J. Damstra
1Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands
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Josiah B. Passmore
1Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands
2Centre for Living Technologies, Alliance TU/e, WUR, UU, UMC Utrecht, Princetonlaan 6, 3584 CB Utrecht, The Netherlands
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Albert K. Serweta
1Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands
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Ioannis Koutlas
3Department of Translational Neuroscience, Brain Center, UMC Utrecht, Utrecht University, Utrecht, The Netherlands
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Mithila Burute
1Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands
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Frank J. Meye
3Department of Translational Neuroscience, Brain Center, UMC Utrecht, Utrecht University, Utrecht, The Netherlands
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Anna Akhmanova
1Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands
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Lukas C. Kapitein
1Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands
2Centre for Living Technologies, Alliance TU/e, WUR, UU, UMC Utrecht, Princetonlaan 6, 3584 CB Utrecht, The Netherlands
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  • For correspondence: l.kapitein@uu.nl
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ABSTRACT

Expansion microscopy (ExM) is a powerful technique to overcome the diffraction limit of light microscopy by physically expanding biological specimen in three dimensions. Nonetheless, using ExM for quantitative or diagnostic applications requires robust quality control methods to precisely determine expansion factors and to map deformations due to anisotropic expansion. Here we present GelMap, a flexible workflow to introduce a fluorescent grid into pre-expanded hydrogels that scales with expansion and reports deformations. We demonstrate that GelMap can be used to precisely determine the local expansion factor and to correct for deformations without the use of cellular reference structures or pre-expansion ground truth images. Moreover, we show that GelMap aids sample navigation for correlative uses of expansion microscopy. Finally, we show that GelMap is compatible with expansion of tissue and can be readily implemented as a quality control step into existing ExM workflows.

Competing Interest Statement

H.G.J.D., J.B.P. and L.C.K have filed a patent application covering the presented methods.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted December 22, 2022.
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GelMap: Intrinsic calibration and deformation mapping for expansion microscopy
Hugo G.J. Damstra, Josiah B. Passmore, Albert K. Serweta, Ioannis Koutlas, Mithila Burute, Frank J. Meye, Anna Akhmanova, Lukas C. Kapitein
bioRxiv 2022.12.21.521394; doi: https://doi.org/10.1101/2022.12.21.521394
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GelMap: Intrinsic calibration and deformation mapping for expansion microscopy
Hugo G.J. Damstra, Josiah B. Passmore, Albert K. Serweta, Ioannis Koutlas, Mithila Burute, Frank J. Meye, Anna Akhmanova, Lukas C. Kapitein
bioRxiv 2022.12.21.521394; doi: https://doi.org/10.1101/2022.12.21.521394

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