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DNA nanopores as artificial membrane channels for bioprotonics

Author

Listed:
  • Le Luo

    (University of California, Santa Cruz)

  • Swathi Manda

    (Massachusetts Institute of Technology)

  • Yunjeong Park

    (University of California, Santa Cruz)

  • Busra Demir

    (TOBB University of Economics and Technology
    TOBB University of Economics and Technology
    University of Washington)

  • Jesse Sanchez

    (University of California, Santa Cruz
    Oregon State University)

  • M. P. Anantram

    (University of Washington)

  • Ersin Emre Oren

    (TOBB University of Economics and Technology
    TOBB University of Economics and Technology)

  • Ashwin Gopinath

    (Massachusetts Institute of Technology)

  • Marco Rolandi

    (University of California, Santa Cruz
    University of California Santa Cruz
    University of California Santa Cruz)

Abstract

Biological membrane channels mediate information exchange between cells and facilitate molecular recognition. While tuning the shape and function of membrane channels for precision molecular sensing via de-novo routes is complex, an even more significant challenge is interfacing membrane channels with electronic devices for signal readout, which results in low efficiency of information transfer - one of the major barriers to the continued development of high-performance bioelectronic devices. To this end, we integrate membrane spanning DNA nanopores with bioprotonic contacts to create programmable, modular, and efficient artificial ion-channel interfaces. Here we show that cholesterol modified DNA nanopores spontaneously and with remarkable affinity span the lipid bilayer formed over the planar bio-protonic electrode surface and mediate proton transport across the bilayer. Using the ability to easily modify DNA nanostructures, we illustrate that this bioprotonic device can be programmed for electronic recognition of biomolecular signals such as presence of Streptavidin and the cardiac biomarker B-type natriuretic peptide, without modifying the biomolecules. We anticipate this robust interface will allow facile electronic measurement and quantification of biomolecules in a multiplexed manner.

Suggested Citation

  • Le Luo & Swathi Manda & Yunjeong Park & Busra Demir & Jesse Sanchez & M. P. Anantram & Ersin Emre Oren & Ashwin Gopinath & Marco Rolandi, 2023. "DNA nanopores as artificial membrane channels for bioprotonics," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40870-1
    DOI: 10.1038/s41467-023-40870-1
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    References listed on IDEAS

    as
    1. Zahra Hemmatian & Scott Keene & Erik Josberger & Takeo Miyake & Carina Arboleda & Jessica Soto-Rodríguez & François Baneyx & Marco Rolandi, 2016. "Electronic control of H+ current in a bioprotonic device with Gramicidin A and Alamethicin," Nature Communications, Nature, vol. 7(1), pages 1-8, December.
    2. Tao Jiang & Aaron Hall & Marco Eres & Zahra Hemmatian & Baofu Qiao & Yun Zhou & Zhiyuan Ruan & Andrew D. Couse & William T. Heller & Haiyan Huang & Monica Olvera de la Cruz & Marco Rolandi & Ting Xu, 2020. "Single-chain heteropolymers transport protons selectively and rapidly," Nature, Nature, vol. 577(7789), pages 216-220, January.
    3. Vishal Maingi & Jonathan R. Burns & Jaakko J. Uusitalo & Stefan Howorka & Siewert J. Marrink & Mark S. P. Sansom, 2017. "Stability and dynamics of membrane-spanning DNA nanopores," Nature Communications, Nature, vol. 8(1), pages 1-12, April.
    4. Jared M. Roseman & Jianxun Lin & Siddharth Ramakrishnan & Jacob K. Rosenstein & Kenneth L. Shepard, 2015. "Hybrid integrated biological–solid-state system powered with adenosine triphosphate," Nature Communications, Nature, vol. 6(1), pages 1-6, December.
    5. Shawn M. Douglas & Hendrik Dietz & Tim Liedl & Björn Högberg & Franziska Graf & William M. Shih, 2009. "Self-assembly of DNA into nanoscale three-dimensional shapes," Nature, Nature, vol. 459(7245), pages 414-418, May.
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