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Customizable Live-Cell Imaging Chambers for Multimodal and Multiplex Fluorescence Microscopy

Adam Tepperman, David Jiao Zheng, Maria Abou Taka, Angela Vrieze, Austin Le Lam, View ORCID ProfileBryan Heit
doi: https://doi.org/10.1101/2020.02.19.955971
Adam Tepperman
1Department of Microbiology and Immunology, The University of Western Ontario, London, Ontario, Canada
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David Jiao Zheng
1Department of Microbiology and Immunology, The University of Western Ontario, London, Ontario, Canada
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Maria Abou Taka
1Department of Microbiology and Immunology, The University of Western Ontario, London, Ontario, Canada
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Angela Vrieze
1Department of Microbiology and Immunology, The University of Western Ontario, London, Ontario, Canada
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Austin Le Lam
1Department of Microbiology and Immunology, The University of Western Ontario, London, Ontario, Canada
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Bryan Heit
1Department of Microbiology and Immunology, The University of Western Ontario, London, Ontario, Canada
2Associate Scientist, Robarts Research Institute, London, Ontario, Canada
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  • ORCID record for Bryan Heit
  • For correspondence: bheit@uwo.ca
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Abstract

Using multiple imaging modalities while performing independent experiments in parallel can greatly enhance the throughput of microscopy-based research, but requires provision of appropriate experimental conditions in a format that meets the microscopy’s optical requirements. Although customized imaging chambers can meet these challenges, the difficulty of manufacturing custom chambers and the relatively high cost and design inflexibility of commercial chambers has limited the adoption of this approach. Herein, we demonstrate the use of 3D printing to produce inexpensive, customized live-cell imaging chambers that are compatible with a range of imaging modalities including super-resolution microscopy. In this approach, biocompatible plastics are used to print imaging chambers designed to meet the specific needs of an experiment, followed by adhesion of the printed chamber to a glass coverslip, producing a chamber that is impermeant to liquids and which supports the growth and imaging of cells over multiple days. This approach can also be used to produce moulds for casting PDMS microfluidic devices. The utility of these chambers is demonstrated using designs for multiplex microscopy, imaging under shear, chemotaxis, and general cellular imaging. Together, this approach represents an inexpensive yet highly customizable approach to produce imaging chambers that are compatible with modern microscopy techniques.

Footnotes

  • The manuscript has been re-focused to concentrate more on the multiplex and multimodal microscopy opportunities offered by this method. Additional data highlighting these capabilities is provided, as is additional descriptions of the strengths and weaknesses of the approach. Additional details on some of the analyses and reagents we used have also been included.

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 4.0 International license.
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Posted April 06, 2020.
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Customizable Live-Cell Imaging Chambers for Multimodal and Multiplex Fluorescence Microscopy
Adam Tepperman, David Jiao Zheng, Maria Abou Taka, Angela Vrieze, Austin Le Lam, Bryan Heit
bioRxiv 2020.02.19.955971; doi: https://doi.org/10.1101/2020.02.19.955971
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Customizable Live-Cell Imaging Chambers for Multimodal and Multiplex Fluorescence Microscopy
Adam Tepperman, David Jiao Zheng, Maria Abou Taka, Angela Vrieze, Austin Le Lam, Bryan Heit
bioRxiv 2020.02.19.955971; doi: https://doi.org/10.1101/2020.02.19.955971

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