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dc.contributor.authorSu, Hui
dc.contributor.authorLiu, Han-Yuan
dc.contributor.authorPappa, Anna-Maria
dc.contributor.authorHidalgo, Tania Cecilia
dc.contributor.authorCavassin, Priscila
dc.contributor.authorInal, Sahika
dc.contributor.authorOwens, Róisín M
dc.contributor.authorDaniel, Susan
dc.date.accessioned2019-12-02T10:57:18Z
dc.date.available2019-12-02T10:57:18Z
dc.date.issued2019-10-30
dc.identifier.citationSu, H., Liu, H.-Y., Pappa, A.-M., Hidalgo, T. C., Cavassin, P., Inal, S., … Daniel, S. (2019). Facile Generation of Biomimetic-Supported Lipid Bilayers on Conducting Polymer Surfaces for Membrane Biosensing. ACS Applied Materials & Interfaces. doi:10.1021/acsami.9b10303
dc.identifier.doi10.1021/acsami.9b10303
dc.identifier.urihttp://hdl.handle.net/10754/660357
dc.description.abstractMembrane biosensors that can rapidly sense pathogen interaction and disrupting agents are needed to identify and screen new drugs to combat antibiotic resistance. Bioelectronic devices have the capability to read out both ionic and electrical signals, but their compatibility with biological membranes is somewhat limited. Supported lipid bilayers (SLBs) have served as useful biomimetics for a myriad of research topics involving biological membranes. However, SLBs are traditionally made on inert, rigid, inorganic surfaces. Here, we demonstrate a versatile and facile method for generating SLBs on a conducting polymer device using a solvent-assisted lipid bilayer (SALB) technique. We use this bioelectronic device to form both mammalian and bacterial membrane mimetics to sense the membrane interactions with a bacterial toxin (α-hemolysin) and an antibiotic compound (polymyxin B), respectively. Our results show that we can form high quality bilayers of both types and sense these particular interactions with them, discriminating between pore formation, in the case of α-hemolysin, and disruption of the bilayer, in the case of polymyxin B. The SALB formation method is compatible with many membrane compositions that will not form via common vesicle fusion methods and works well in microfluidic devices. This, combined with the massive parallelization possible for the fabrication of electronic devices, can lead to miniaturized multiplexed devices for rapid data acquisition necessary to identify antibiotic targets that specifically disrupt bacterial, but not mammalian membranes, or identify bacterial toxins that strongly interact with mammalian membranes.
dc.description.sponsorshipWe 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. P.C. would like to acknowledge funding from the Fundaca̧ o de Amparo a ̃ ̀ Pesquisa do Estado de Sao Paulo ̃ (project 2018/14801-9). Research was sponsored by the Defense Advanced Research Projects Agency (DARPA) Army Research Office and was accomplished under Cooperative agreement number W911NF-18-2-0152. 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. The U.S. Government is authorized to reproduce and distribute reprints for Government purposes notwithstanding any copyright notation herein.
dc.publisherAmerican Chemical Society (ACS)
dc.relation.urlhttps://pubs.acs.org/doi/10.1021/acsami.9b10303
dc.titleFacile Generation of Biomimetic-Supported Lipid Bilayers on Conducting Polymer Surfaces for Membrane Biosensing.
dc.typeArticle
dc.contributor.departmentBiological and Environmental Science and Engineering Division , King Abdullah University of Science and Technology (KAUST) , Thuwal , Makkah Province 23955-6900 , Saudi Arabia.
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentBioscience Program
dc.identifier.journalACS applied materials & interfaces
dc.rights.embargodate2020-10-30
dc.eprint.versionPost-print
dc.contributor.institutionRobert F. Smith School of Chemical and Biomolecular Engineering , Cornell University , Ithaca , New York 14853 , United States.
dc.contributor.institutionDepartment of Chemical Engineering and Biotechnology , University of Cambridge , Cambridge CB3 0AS , U.K.
kaust.personHidalgo, Tania Cecilia
kaust.personInal, Sahika
refterms.dateFOA2019-12-04T05:22:21Z


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