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Live single-cell laser tag

Author

Listed:
  • Loïc Binan

    (Research Center of the Maisonneuve-Rosemont Hospital
    Université de Montréal)

  • Javier Mazzaferri

    (Research Center of the Maisonneuve-Rosemont Hospital)

  • Karine Choquet

    (McGill University
    Lady Davis Institute for Medical Research, Jewish General Hospital)

  • Louis-Etienne Lorenzo

    (Institut Universitaire en Santé Mentale de Québec)

  • Yu Chang Wang

    (McGill University and Genome Quebec Innovation Centre)

  • El Bachir Affar

    (Research Center of the Maisonneuve-Rosemont Hospital
    Université de Montréal)

  • Yves De Koninck

    (Institut Universitaire en Santé Mentale de Québec
    Université Laval)

  • Jiannis Ragoussis

    (McGill University
    McGill University and Genome Quebec Innovation Centre
    Center of Innovation in Personalized Medicine, Cancer and Mutagen Unit, King Fahd Center for Medical Research, King Abdulaziz University)

  • Claudia L. Kleinman

    (McGill University
    Lady Davis Institute for Medical Research, Jewish General Hospital)

  • Santiago Costantino

    (Research Center of the Maisonneuve-Rosemont Hospital
    Université de Montréal)

Abstract

The ability to conduct image-based, non-invasive cell tagging, independent of genetic engineering, is key to cell biology applications. Here we introduce cell labelling via photobleaching (CLaP), a method that enables instant, specific tagging of individual cells based on a wide array of criteria such as shape, behaviour or positional information. CLaP uses laser illumination to crosslink biotin onto the plasma membrane, coupled with streptavidin conjugates to label individual cells for genomic, cell-tracking, flow cytometry or ultra-microscopy applications. We show that the incorporated mark is stable, non-toxic, retained for several days, and transferred by cell division but not to adjacent cells in culture. To demonstrate the potential of CLaP for genomic applications, we combine CLaP with microfluidics-based single-cell capture followed by transcriptome-wide next-generation sequencing. Finally, we show that CLaP can also be exploited for inducing transient cell adhesion to substrates for microengineering cultures with spatially patterned cell types.

Suggested Citation

  • Loïc Binan & Javier Mazzaferri & Karine Choquet & Louis-Etienne Lorenzo & Yu Chang Wang & El Bachir Affar & Yves De Koninck & Jiannis Ragoussis & Claudia L. Kleinman & Santiago Costantino, 2016. "Live single-cell laser tag," Nature Communications, Nature, vol. 7(1), pages 1-8, September.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11636
    DOI: 10.1038/ncomms11636
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