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On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device

Author

Listed:
  • M. Rahman

    (University of California Santa Cruz)

  • M. A. Stott

    (Brigham Young University)

  • M. Harrington

    (University of California Santa Cruz)

  • Y. Li

    (University of California Santa Cruz)

  • M. J. N. Sampad

    (University of California Santa Cruz)

  • L. Lancaster

    (University of California at Santa Cruz)

  • T. D. Yuzvinsky

    (University of California Santa Cruz)

  • H. F. Noller

    (University of California at Santa Cruz)

  • A. R. Hawkins

    (Brigham Young University)

  • H. Schmidt

    (University of California Santa Cruz)

Abstract

Nanopore-based single nanoparticle detection has recently emerged as a vibrant research field with numerous high-impact applications. Here, we introduce a programmable optofluidic chip for nanopore-based particle analysis: feedback-controlled selective delivery of a desired number of biomolecules and integration of optical detection techniques on nanopore-selected particles. We demonstrate the feedback-controlled introduction of individual biomolecules, including 70S ribosomes, DNAs and proteins into a fluidic channel where the voltage across the nanopore is turned off after a user-defined number of single molecular insertions. Delivery rates of hundreds/min with programmable off-times of the pore are demonstrated using individual 70S ribosomes. We then use real-time analysis of the translocation signal for selective voltage gating of specific particles from a mixture, enabling selection of DNAs from a DNA-ribosome mixture. Furthermore, we report optical detection of nanopore-selected DNA molecules. These capabilities point the way towards a powerful research tool for high-throughput single-molecule analysis on a chip.

Suggested Citation

  • M. Rahman & M. A. Stott & M. Harrington & Y. Li & M. J. N. Sampad & L. Lancaster & T. D. Yuzvinsky & H. F. Noller & A. R. Hawkins & H. Schmidt, 2019. "On demand delivery and analysis of single molecules on a programmable nanopore-optofluidic device," Nature Communications, Nature, vol. 10(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11723-7
    DOI: 10.1038/s41467-019-11723-7
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