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Self-Assembly of Mammalian-Cell Membranes on Bioelectronic Devices with Functional Transmembrane Proteins.
Liu, Han-Yuan; Pappa, Anna-Maria; Pavia, Aimie; Pitsalidis, Charalampos; Thiburce, Quentin; Salleo, Alberto; Owens, Róisín M; Daniel, Susan.
Afiliación
  • Liu HY; Robert F. Smith School of Chemical and Biomolecular Engineering, Cornell University, Olin Hall, Ithaca, New York 14853, United States.
  • Pappa AM; Department of Chemical Engineering and BiotechnologyUniversity of Cambridge, Philippa Fawcett Drive, CB30AS Cambridge, UK.
  • Pavia A; Department of Flexible Electronics, Ecole Nationale Supérieure des Mines, CMP-EMSE, 13541 Gardanne, France.
  • Pitsalidis C; Panaxium SAS, 13100 Aix-en-Provence, France.
  • Thiburce Q; Department of Chemical Engineering and BiotechnologyUniversity of Cambridge, Philippa Fawcett Drive, CB30AS Cambridge, UK.
  • Salleo A; Department of Materials Science and Engineering, Stanford University, 496 Lomita Mall, Stanford, California 94305, United States.
  • Owens RM; Department of Materials Science and Engineering, Stanford University, 496 Lomita Mall, Stanford, California 94305, United States.
  • Daniel S; Department of Chemical Engineering and BiotechnologyUniversity of Cambridge, Philippa Fawcett Drive, CB30AS Cambridge, UK.
Langmuir ; 36(26): 7325-7331, 2020 07 07.
Article en En | MEDLINE | ID: mdl-32388991
ABSTRACT
Transmembrane proteins (TMPs) regulate processes occurring at the cell surface and are essential gatekeepers of information flow across the membrane. TMPs are difficult to study, given the complex environment of the membrane and its influence on protein conformation, mobility, biomolecule interaction, and activity. For the first time, we create mammalian biomembranes supported on a transparent, electrically conducting polymer surface, which enables dual electrical and optical monitoring of TMP function in its native membrane environment. Mammalian plasma membrane vesicles containing ATP-gated P2X2 ion channels self-assemble on a biocompatible polymer cushion that transduces the changes in ion flux during ATP exposure. This platform maintains the complexity of the native plasma membrane, the fluidity of its constituents, and protein orientation critical to ion channel function. We demonstrate the dual-modality readout using microscopy to characterize protein mobility by single-particle tracking and sensing of ATP gating of P2X2 using electrical impedance spectroscopy. This measurement of TMP activity important for pain sensing, neurological activity, and sensory activity raises new possibilities for drug screening and biosensing applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canales Iónicos / Proteínas de la Membrana Límite: Animals Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canales Iónicos / Proteínas de la Membrana Límite: Animals Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos