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Multiplexed and millimeter-scale superresolution imaging of cells and tissue sections via prism-illumination and microfluidics-enhanced DNA-PAINT

Matthew J Rames, John Kenison, Daniel Heineck, Fehmi Civitci, Malwina Szczepaniak, Kai Tao, Ting Zheng, Julia Shangguan, Sadik Esener, View ORCID ProfileXiaolin Nan
doi: https://doi.org/10.1101/2022.08.07.503091
Matthew J Rames
1Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, 2720 S Moody Ave., Portland, OR 97201, USA
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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John Kenison
1Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, 2720 S Moody Ave., Portland, OR 97201, USA
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Daniel Heineck
1Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, 2720 S Moody Ave., Portland, OR 97201, USA
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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Fehmi Civitci
1Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, 2720 S Moody Ave., Portland, OR 97201, USA
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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Malwina Szczepaniak
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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Kai Tao
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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Ting Zheng
1Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, 2720 S Moody Ave., Portland, OR 97201, USA
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Julia Shangguan
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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Sadik Esener
1Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, 2720 S Moody Ave., Portland, OR 97201, USA
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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Xiaolin Nan
1Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health & Science University, 2720 S Moody Ave., Portland, OR 97201, USA
2Program in Quantitative and Systems Biology, Department of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, OR 97201, USA
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  • ORCID record for Xiaolin Nan
  • For correspondence: nan@ohsu.edu
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Abstract

Superresolution microscopy (SRM) has been an enabling tool for biomedical research. A major limitation of SRM, however, is the small field-of-view (FOV), typically ~50μm x 50μm and up to ~200μm x 200μm in recent attempts, hampering its use in imaging large cell populations or clinical tissues. Here we report PRism-Illumination and Microfluidics-Enhanced DNA-PAINT (PRIME-PAINT) for efficient, multiplexed SRM across millimeter-scale FOVs. Unlike existing SRM, PRIME-PAINT uses prism-type illumination for robust DNA-PAINT with single FOVs up to a half millimeter. Through stitching, imaging over mm2 FOVs can be completed in under an hour per target. The on-stage microfluidics not only facilitates multiplexing but enhances image quality, particularly for tissue sections. We demonstrate the utility of PRIME-PAINT by analyzing ~106 caveolae structures in ~1,000 cells and imaging entire pancreatic cancer lesions from patient tissue biopsies. Thus, we expect PRIME-PAINT to be useful toward building multiscale, Google-Earth-like views of biological systems.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Added a new data figure (new Fig. S3) to demonstrate stitching of multiple 0.5 x 0.5 mm2 field-of-views (FOVs) to achieve 1 mm2 FOV within less than an hour. Other supplementary figures were re-numbered accordingly. Relevant statements in the abstract and main text were updated. Overall the changes were minor.

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-ND 4.0 International license.
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Posted August 31, 2022.
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Multiplexed and millimeter-scale superresolution imaging of cells and tissue sections via prism-illumination and microfluidics-enhanced DNA-PAINT
Matthew J Rames, John Kenison, Daniel Heineck, Fehmi Civitci, Malwina Szczepaniak, Kai Tao, Ting Zheng, Julia Shangguan, Sadik Esener, Xiaolin Nan
bioRxiv 2022.08.07.503091; doi: https://doi.org/10.1101/2022.08.07.503091
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Multiplexed and millimeter-scale superresolution imaging of cells and tissue sections via prism-illumination and microfluidics-enhanced DNA-PAINT
Matthew J Rames, John Kenison, Daniel Heineck, Fehmi Civitci, Malwina Szczepaniak, Kai Tao, Ting Zheng, Julia Shangguan, Sadik Esener, Xiaolin Nan
bioRxiv 2022.08.07.503091; doi: https://doi.org/10.1101/2022.08.07.503091

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