TY - JOUR
T1 - Creating Biological Membranes on the Micron Scale
T2 - Forming Patterned Lipid Bilayers Using a Polymer Lift-Off Technique
AU - Orth, R. N.
AU - Kameoka, J.
AU - Zipfel, W. R.
AU - Ilic, B.
AU - Webb, W. W.
AU - Clark, T. G.
AU - Craighead, H. G.
N1 - Funding Information:
This work was supported by the Defense Advanced Research Projects Agency, the Nanobiotechnology Center (NBTC, a Science and Technology Centers program of the National Science Foundation under Agreement ECS-9876771), the resources of the Cornell Nanofabrication Facility, and the United States Air Force. The views expressed in this article are those of the authors and do not reflect the official policy or position of the U.S. Air Force, Department of Defense, or the U.S. government.
Funding Information:
W.R.Z. and W.W.W. acknowledge support from grant P41-RR04224 from the National Center for Research Resources, National Institutes of Health. We also thank several individuals at Cornell University for their insight and research assistance: Drs. Holowka and Baird for their guidance on forming supported lipid bilayers, Dr. Stephen W. Turner for his assistance with image analysis and pattern design, Dr. Ismail Hafez for assistance preparing the lipids, Dr. Erin Sheets for advice on how to prepare lipids, Min Wu for supplying the Alexa 488 monoclonal mouse anti-DNP antibody, and Jennifer Gaudioso for her manuscript review.
PY - 2003/11
Y1 - 2003/11
N2 - We present a new method for creating patches of fluid lipid bilayers with conjugated biotin and other compounds down to 1 μm resolution using a photolithographically patterned polymer lift-off technique. The patterns are realized as the polymer is mechanically peeled away in one contiguous piece in solution. The functionality of these surfaces is verified with binding of antibodies and avidin on these uniform micron-scale platforms. The biomaterial patches, measuring 1 μm-76 μm on edge, provide a synthetic biological substrate for biochemical analysis that is ∼100× smaller in width than commercial printing technologies. 100 nm unilamellar lipid vesicles spread to form a supported fluid lipid bilayer on oxidized silicon surface as confirmed by fluorescence photobleaching recovery. Fluorescence photobleaching recovery measurements of Dil (1,1′-dioctadecyl-3,3,3′,3′ -tetramethylindocarbocyanine perchlorate (DiIC18(3))) stained bilayer patches yielded an average diffusion coefficient of 7.54 ± 1.25 μm2 s-1, equal to or slightly faster than typically found in Dil stained cells. This diffusion rate is ∼3× faster than previous values for bilayers on glass. This method provides a new means to form functionalized fluid lipid bilayers as micron-scale platforms to immobilize biomaterials, capture antibodies and biotinylated reagents from solution, and form antigenic stimuli for cell stimulation.
AB - We present a new method for creating patches of fluid lipid bilayers with conjugated biotin and other compounds down to 1 μm resolution using a photolithographically patterned polymer lift-off technique. The patterns are realized as the polymer is mechanically peeled away in one contiguous piece in solution. The functionality of these surfaces is verified with binding of antibodies and avidin on these uniform micron-scale platforms. The biomaterial patches, measuring 1 μm-76 μm on edge, provide a synthetic biological substrate for biochemical analysis that is ∼100× smaller in width than commercial printing technologies. 100 nm unilamellar lipid vesicles spread to form a supported fluid lipid bilayer on oxidized silicon surface as confirmed by fluorescence photobleaching recovery. Fluorescence photobleaching recovery measurements of Dil (1,1′-dioctadecyl-3,3,3′,3′ -tetramethylindocarbocyanine perchlorate (DiIC18(3))) stained bilayer patches yielded an average diffusion coefficient of 7.54 ± 1.25 μm2 s-1, equal to or slightly faster than typically found in Dil stained cells. This diffusion rate is ∼3× faster than previous values for bilayers on glass. This method provides a new means to form functionalized fluid lipid bilayers as micron-scale platforms to immobilize biomaterials, capture antibodies and biotinylated reagents from solution, and form antigenic stimuli for cell stimulation.
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U2 - 10.1016/S0006-3495(03)74725-0
DO - 10.1016/S0006-3495(03)74725-0
M3 - Article
C2 - 14581207
AN - SCOPUS:0242385353
SN - 0006-3495
VL - 85
SP - 3066
EP - 3073
JO - Biophysical Journal
JF - Biophysical Journal
IS - 5
ER -