Electronic control of H+ current in a bioprotonic device with Gramicidin A and Alamethicin
Abstract
In biological systems, intercellular communication is mediated by membrane proteins and ion channels that regulate traffic of ions and small molecules across cell membranes. A bioelectronic device with ion channels that control ionic flow across a supported lipid bilayer (SLB) should therefore be ideal for interfacing with biological systems. Here, we demonstrate a biotic–abiotic bioprotonic device with Pd contacts that regulates proton (H+) flow across an SLB incorporating the ion channels Gramicidin A (gA) and Alamethicin (ALM). We model the device characteristics using the Goldman–Hodgkin–Katz (GHK) solution to the Nernst–Planck equation for transport across the membrane. We derive the permeability for an SLB integrating gA and ALM and demonstrate pH control as a function of applied voltage and membrane permeability. This work opens the door to integrating more complex H+ channels at the Pd contact interface to produce responsive biotic–abiotic devices with increased functionality.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Oct 07, 2016
- Source ID
- 10.1038/ncomms12981
Entities
People
- Carina Arboleda
- Erik E Josberger
- François Baneyx
- Jessica Soto-rodríguez
- Marco Rolandi
- Scott Keene
- Takeo Miyake
- Zahra Hemmatian