TY - JOUR
T1 - Self-aligned supported lipid bilayers for patterning the cell-substrate interface
AU - Shen, Keyue
AU - Tsai, Jones
AU - Shi, Peng
AU - Kam, Lance C.
PY - 2009/9/23
Y1 - 2009/9/23
N2 - (Figure Presented) Supported lipid bilayers capture the fluidity and chemical properties of cellular membranes. In this report, we introduce a method for creating surfaces that contain multiple, aligned regions of supported membranes of different compositions at scales of micrometers and smaller. This method uses the design of a diffusional barrier to increase the resolution that can be achieved directly using traditional bilayer patterning techniques, such as laminar flow. We demonstrate the use of this platform for presenting ligands to the T Cell Receptor and LFA-1 that are tethered to separate, closely juxtaposed regions of bilayer, capturing an important aspect of the natural organization observed between T cells and Antigen Presenting Cells. Our results present a novel platform for the study of spatial separation of extracellular ligands and its impact on cell signals. © 2009 American Chemical Society.
AB - (Figure Presented) Supported lipid bilayers capture the fluidity and chemical properties of cellular membranes. In this report, we introduce a method for creating surfaces that contain multiple, aligned regions of supported membranes of different compositions at scales of micrometers and smaller. This method uses the design of a diffusional barrier to increase the resolution that can be achieved directly using traditional bilayer patterning techniques, such as laminar flow. We demonstrate the use of this platform for presenting ligands to the T Cell Receptor and LFA-1 that are tethered to separate, closely juxtaposed regions of bilayer, capturing an important aspect of the natural organization observed between T cells and Antigen Presenting Cells. Our results present a novel platform for the study of spatial separation of extracellular ligands and its impact on cell signals. © 2009 American Chemical Society.
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U2 - 10.1021/ja904721h
DO - 10.1021/ja904721h
M3 - RGC 21 - Publication in refereed journal
C2 - 19708648
SN - 0002-7863
VL - 131
SP - 13204
EP - 13205
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 37
ER -