Versatile Bottom-Up Synthesis of Tethered Bilayer Lipid Membranes on Nanoelectronic Biosensor Devices.

ACS Appl Mater Interfaces

Integrated Nanosystems Research Facility, Department of Electrical Engineering and Computer Science, University of California at Irvine, Irvine, California 92697, United States.

Published: May 2017

AI Article Synopsis

  • Interfacing nanoelectronic devices with cell membranes allows for the detailed detection of biological processes at the single ion channel level, which can enhance applications in pharmacology and clinical diagnostics.
  • The study introduces a straightforward method to create tethered bilayer lipid membranes (tBLMs) on silicon and glass surfaces using a series of simple chemical reactions, making it accessible for many research laboratories.
  • The successful integration of tBLMs with various nanoelectronic sensors demonstrates real-time monitoring of single ion channel activity, highlighting the potential for improved sensitivity and resolution in biological measurements.

Article Abstract

Interfacing nanoelectronic devices with cell membranes can enable multiplexed detection of fundamental biological processes (such as signal transduction, electrophysiology, and import/export control) even down to the single ion channel level, which can lead to a variety of applications in pharmacology and clinical diagnosis. Therefore, it is necessary to understand and control the chemical and electrical interface between the device and the lipid bilayer membrane. Here, we develop a simple bottom-up approach to assemble tethered bilayer lipid membranes (tBLMs) on silicon wafers and glass slides, using a covalent tether attachment chemistry based on silane functionalization, followed by step-by-step stacking of two other functional molecular building blocks (oligo-poly(ethylene glycol) (PEG) and lipid). A standard vesicle fusion process was used to complete the bilayer formation. The monolayer synthetic scheme includes three well-established chemical reactions: self-assembly, epoxy-amine reaction, and EDC/NHS cross-linking reaction. All three reactions are facile and simple and can be easily implemented in many research labs, on the basis of common, commercially available precursors using mild reaction conditions. The oligo-PEG acts as the hydrophilic spacer, a key role in the formation of a homogeneous bilayer membrane. To explore the broad applicability of this approach, we have further demonstrated the formation of tBLMs on three common classes of (nano)electronic biosensor devices: indium-tin oxide-coated glass, silicon nanoribbon devices, and high-density single-walled carbon nanotubes (SWNT) networks on glass. More importantly, we incorporated alemethicin into tBLMs and realized the real-time recording of single ion channel activity with high sensitivity and high temporal resolution using the tBLMs/SWNT network transistor hybrid platform. This approach can provide a covalently bonded lipid coating on the oxide layer of nanoelectronic devices, which will enable a variety of applications in the emerging field of nanoelectronic interfaces to electrophysiology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373873PMC
http://dx.doi.org/10.1021/acsami.7b00268DOI Listing

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