Membrane 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.