Abstract
Black lipid membranes (BLMs) provide a synthetic environment that facilitates measurement of ion channel activity in diverse analytical platforms. The limited electrical, mechanical and temporal stabilities of BLMs pose a significant challenge to development of highly stable measurement platforms. Here, ethylene glycol dimethacrylate (EGDMA) and butyl methacrylate (BMA) were partitioned into BLMs and photopolymerized to create a cross-linked polymer scaffold in the bilayer lamella that dramatically improved BLM stability. The commercially available methacrylate monomers provide a simple, low cost, and broadly accessible approach for preparing highly stabilized BLMs useful for ion channel-functionalized analytical platforms. When prepared on silane-modified glass microapertures, the resulting polymer scaffold-stabilized (PSS)-BLMs exhibited significantly improved lifetimes of 23 ± 9 to 40 ± 14 h and >10-fold increase in mechanical stability, with breakdown potentials >2000 mV attainable, depending on surface modification and polymer cross-link density. Additionally, the polymer scaffold exerted minimal perturbation to membrane electrical integrity as indicated by mean conductance measurements. When gramicidin A and α-hemolysin were reconstituted into PSS-BLMs, the ion channels retained function comparable to conventional BLMs. This approach is a key advance in the formation of stabilized BLMs and should be amenable to a wide range of receptor and ion channel functionalized platforms.
Original language | English (US) |
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Pages (from-to) | 955-963 |
Number of pages | 9 |
Journal | ACS Biomaterials Science and Engineering |
Volume | 1 |
Issue number | 10 |
DOIs | |
State | Published - Oct 12 2015 |
Keywords
- black lipid membrane
- gramicidin
- ion channel
- lipid bilayer
- methacrylate polymer
- polymer scaffold
- α-hemolysin
ASJC Scopus subject areas
- Biomaterials
- Biomedical Engineering