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A semiconductor 96-microplate platform for electrical-imaging based high-throughput phenotypic screening

Author

Listed:
  • Shalaka Chitale

    (CytoTronics Inc.)

  • Wenxuan Wu

    (CytoTronics Inc.
    Harvard University)

  • Avik Mukherjee

    (Harvard Medical School)

  • Herbert Lannon

    (CytoTronics Inc.)

  • Pooja Suresh

    (CytoTronics Inc.)

  • Ishan Nag

    (CytoTronics Inc.)

  • Christina M. Ambrosi

    (CytoTronics Inc.)

  • Rona S. Gertner

    (Harvard University)

  • Hendrick Melo

    (CytoTronics Inc.)

  • Brendan Powers

    (CytoTronics Inc.)

  • Hollin Wilkins

    (CytoTronics Inc.)

  • Henry Hinton

    (Harvard University)

  • Michael Cheah

    (CytoTronics Inc.)

  • Zachariah G. Boynton

    (CytoTronics Inc.)

  • Alexander Alexeyev

    (CytoTronics Inc.)

  • Duane Sword

    (CytoTronics Inc.)

  • Markus Basan

    (Harvard Medical School)

  • Hongkun Park

    (Harvard University
    Harvard University)

  • Donhee Ham

    (Harvard University)

  • Jeffrey Abbott

    (CytoTronics Inc.
    Harvard University
    Harvard University
    Harvard University)

Abstract

High-content imaging for compound and genetic profiling is popular for drug discovery but limited to endpoint images of fixed cells. Conversely, electronic-based devices offer label-free, live cell functional information but suffer from limited spatial resolution or throughput. Here, we introduce a semiconductor 96-microplate platform for high-resolution, real-time impedance imaging. Each well features 4096 electrodes at 25 µm spatial resolution and a miniaturized data interface allows 8× parallel plate operation (768 total wells) for increased throughput. Electric field impedance measurements capture >20 parameter images including cell barrier, attachment, flatness, and motility every 15 min during experiments. We apply this technology to characterize 16 cell types, from primary epithelial to suspension cells, and quantify heterogeneity in mixed co-cultures. Screening 904 compounds across 13 semiconductor microplates reveals 25 distinct responses, demonstrating the platform’s potential for mechanism of action profiling. The scalability and translatability of this semiconductor platform expands high-throughput mechanism of action profiling and phenotypic drug discovery applications.

Suggested Citation

  • Shalaka Chitale & Wenxuan Wu & Avik Mukherjee & Herbert Lannon & Pooja Suresh & Ishan Nag & Christina M. Ambrosi & Rona S. Gertner & Hendrick Melo & Brendan Powers & Hollin Wilkins & Henry Hinton & Mi, 2023. "A semiconductor 96-microplate platform for electrical-imaging based high-throughput phenotypic screening," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43333-9
    DOI: 10.1038/s41467-023-43333-9
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    References listed on IDEAS

    as
    1. Ernest Latorre & Sohan Kale & Laura Casares & Manuel Gómez-González & Marina Uroz & Léo Valon & Roshna V. Nair & Elena Garreta & Nuria Montserrat & Aránzazu Campo & Benoit Ladoux & Marino Arroyo & Xav, 2018. "Active superelasticity in three-dimensional epithelia of controlled shape," Nature, Nature, vol. 563(7730), pages 203-208, November.
    2. Mohammad Ikbal Choudhury & Yizeng Li & Panagiotis Mistriotis & Ana Carina N. Vasconcelos & Eryn E. Dixon & Jing Yang & Morgan Benson & Debonil Maity & Rebecca Walker & Leigha Martin & Fatima Koroma & , 2022. "Kidney epithelial cells are active mechano-biological fluid pumps," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
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