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    Biomembrane-based organic electronic devices for ligand-receptor binding studies.

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    Liu et. al manuscript ABC invited submission accepted version.pdf
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    Type
    Article
    Authors
    Liu, Han-Yuan
    Pappa, Anna-Maria
    Hidalgo, Tania Cecilia
    Inal, Sahika cc
    Owens, Rόisín M
    Daniel, Susan cc
    KAUST Department
    Biological and Environmental Sciences and Engineering (BESE) Division
    Bioscience Program
    Date
    2020-02-05
    Online Publication Date
    2020-02-05
    Print Publication Date
    2020-09
    Embargo End Date
    2021-02-06
    Submitted Date
    2019-12-02
    Permanent link to this record
    http://hdl.handle.net/10754/661484
    
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    Abstract
    We present a simple, rapid method for forming supported lipid bilayers on organic electronic devices composed of conducting polymer electrodes using a solvent-assisted lipid bilayer formation method. These supported bilayers present protein recognition elements that are mobile, critical for multivalent binding interactions. Because these polymers are transparent and conducting, we demonstrate, by optical and electrical detection, the specific interactions of proteins with these biomembrane-based bioelectronic devices. This work paves the way for easy formation of biomembrane mimetics for sensing and detection of binding events in a label-free manner on organic electronic devices of more sophisticated architectures. Graphical abstract.
    Citation
    Liu, H.-Y., Pappa, A.-M., Hidalgo, T. C., Inal, S., Owens, R. M., & Daniel, S. (2020). Biomembrane-based organic electronic devices for ligand–receptor binding studies. Analytical and Bioanalytical Chemistry. doi:10.1007/s00216-020-02449-3
    Sponsors
    We thank Professor Nam-Joon Cho (the Engineering in Translational Science Group at Nanyang Technical University) for his advice and providing the microfluidic flow cells used in this work. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the official policies, either expressed or implied, of DARPA or the Army Research Office or the U.S.Government.
    A.M.P. received funding from the Oppenheimer Junior Research Fellowship. Part of this work was supported by the King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) under Award No. OSR-2018-CRG7-3709. This research was sponsored in part by the Defense Advanced Research Projects Agency (DARPA) Army Research Office and was accomplished under Cooperative agreement number W911NF-18-2-0152.
    Publisher
    Springer Nature
    Journal
    Analytical and bioanalytical chemistry
    DOI
    10.1007/s00216-020-02449-3
    Additional Links
    http://link.springer.com/10.1007/s00216-020-02449-3
    ae974a485f413a2113503eed53cd6c53
    10.1007/s00216-020-02449-3
    Scopus Count
    Collections
    Articles; Biological and Environmental Science and Engineering (BESE) Division; Bioscience Program

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