TY - JOUR
T1 - Fluidic and air-stable supported lipid bilayer and cell-mimicking microarrays
AU - Deng, Yang
AU - Wang, Yini
AU - Holtz, Bryan
AU - Li, Jingyi
AU - Traaseth, Nathan
AU - Veglia, Gianluigi
AU - Stottrup, Benjamin J.
AU - Elde, Robert
AU - Pei, Duanqing
AU - Guo, Athena
AU - Zhu, X. Y.
PY - 2008/5/14
Y1 - 2008/5/14
N2 - As drug delivery, therapy, and medical imaging are becoming increasingly cell-specific, there is a critical need for high fidelity and high-throughput screening methods for cell surface interactions. Cell membrane-mimicking surfaces, i.e., supported lipid bilayers (SLBs), are currently not sufficiently robust to meet this need. Here we describe a method of forming fluidic and air-stable SLBs through tethered and dispersed cholesterol groups incorporated into the bottom leaflet. Achieving air stability allows us to easily fabricate SLB microarrays from direct robotic spotting of vesicle solutions. We demonstrate their application as cell membrane-mimicking microarrays by reconstituting peripheral as well as integral membrane components that can be recognized by their respective targets. These demonstrations establish the viability of the fluidic and air-stable SLB platform for generating content microarrays in high throughput studies, e.g., the screening of drugs and nanomedicine targeting cell surface receptors.
AB - As drug delivery, therapy, and medical imaging are becoming increasingly cell-specific, there is a critical need for high fidelity and high-throughput screening methods for cell surface interactions. Cell membrane-mimicking surfaces, i.e., supported lipid bilayers (SLBs), are currently not sufficiently robust to meet this need. Here we describe a method of forming fluidic and air-stable SLBs through tethered and dispersed cholesterol groups incorporated into the bottom leaflet. Achieving air stability allows us to easily fabricate SLB microarrays from direct robotic spotting of vesicle solutions. We demonstrate their application as cell membrane-mimicking microarrays by reconstituting peripheral as well as integral membrane components that can be recognized by their respective targets. These demonstrations establish the viability of the fluidic and air-stable SLB platform for generating content microarrays in high throughput studies, e.g., the screening of drugs and nanomedicine targeting cell surface receptors.
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U2 - 10.1021/ja800049f
DO - 10.1021/ja800049f
M3 - Article
C2 - 18407640
AN - SCOPUS:43249095010
SN - 0002-7863
VL - 130
SP - 6267
EP - 6271
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 19
ER -