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Low cost and massively parallel force spectroscopy with fluid loading on a chip

Author

Listed:
  • Ehsan Akbari

    (The Ohio State University
    The Ohio State University)

  • Melika Shahhosseini

    (The Ohio State University)

  • Ariel Robbins

    (The Ohio State University
    The Ohio State University)

  • Michael G. Poirier

    (The Ohio State University
    The Ohio State University
    The Ohio State University)

  • Jonathan W. Song

    (The Ohio State University
    The Ohio State University)

  • Carlos E. Castro

    (The Ohio State University
    The Ohio State University)

Abstract

Current approaches for single molecule force spectroscopy are typically constrained by low throughput and high instrumentation cost. Herein, a low-cost, high throughput technique is demonstrated using microfluidics for multiplexed mechanical manipulation of up to ~4000 individual molecules via molecular fluid loading on-a-chip (FLO-Chip). The FLO-Chip consists of serially connected microchannels with varying width, allowing for simultaneous testing at multiple loading rates. Molecular force measurements are demonstrated by dissociating Biotin-Streptavidin and Digoxigenin-AntiDigoxigenin interactions along with unzipping of double stranded DNA of varying sequence under different dynamic loading rates and solution conditions. Rupture force results under varying loading rates and solution conditions are in good agreement with prior studies, verifying a versatile approach for single molecule biophysics and molecular mechanobiology. FLO-Chip enables straightforward, rapid, low-cost, and portable mechanical testing of single molecules that can be implemented on a wide range of microscopes to broaden access and may enable new applications of molecular force spectroscopy.

Suggested Citation

  • Ehsan Akbari & Melika Shahhosseini & Ariel Robbins & Michael G. Poirier & Jonathan W. Song & Carlos E. Castro, 2022. "Low cost and massively parallel force spectroscopy with fluid loading on a chip," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34212-w
    DOI: 10.1038/s41467-022-34212-w
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    References listed on IDEAS

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