4.8 Article

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

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 17, 页码 14618-14632

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b00268

关键词

tethered bilayer lipid membranes; silicon wafer; glass slide; indium-tin oxide; silicon nanoribbon; single-walled carbon nanotube film; biosensor

资金

  1. Army Research Office through the ARO-MURI program
  2. ARO [MURI W911NF-11-1-0024, ARO W911NF-09-1-0319, DURIP W911NF-11-1-0315]
  3. NIH [NIH IMAT R33CA183384]
  4. University of California, Irvine [ca-62203]
  5. National Science Foundation Major Research Instrumentation Program [CHE-1338173]

向作者/读者索取更多资源

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, arid 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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