Department of Chemistry, University of Arizona, 1306 E. University Boulevard, Tucson, Arizona 85721, USA.
ACS Appl Mater Interfaces. 2009 Jun;1(6):1310-5. doi: 10.1021/am900177p.
A continuous-flow microspotter was used to generate planar arrays of stabilized bilayers composed of the polymerizable lipid bis-SorbPC and dopant lipids bearing ligands for proteins. Fluorescence microscopy was used to determine the uniformity of the bilayers and to detect protein binding. After UV-initiated polymerization, poly(lipid) bilayer microarrays were air-stable. Cholera toxin subunit b (CTb) bound to an array of poly(lipid) bilayers doped with GM(1), and the extent of binding was correlated to the mole percentage of GM(1) in each spot. A poly(lipid) bilayer array composed of spots doped with GM(1) and spots doped with biotin-DOPE specifically bound CTb and streptavidin to the respective spots from a dissolved mixture of the two proteins. Poly(bis-SorbPC)/GM(1) arrays retained specific CTb binding capacity after multiple regenerations with a protein denaturing solution and also after exposure to air. In addition, these arrays are stable in vacuum, which allows the use of MALDI-TOF mass spectrometry to detect specifically bound CTb. This work demonstrates the considerable potential of poly(lipid) bilayer arrays for high-throughput binding assays and lipidomics studies.
连续流动微点样器用于生成由可聚合脂质双 SorbPC 和带有蛋白质配体的掺杂脂质组成的稳定双层的平面阵列。荧光显微镜用于确定双层的均匀性并检测蛋白质结合。在 UV 引发聚合后,聚(脂质)双层微阵列具有空气稳定性。霍乱毒素亚基 b (CTb) 与掺杂 GM(1) 的聚(脂质)双层阵列结合,结合程度与每个斑点中 GM(1)的摩尔百分比相关。由掺杂 GM(1)的斑点和掺杂生物素-DOPE 的斑点组成的聚(脂质)双层阵列特异性地将 CTb 和链霉亲和素结合到两种蛋白质溶解混合物的相应斑点上。由聚(双 SorbPC)/GM(1) 阵列组成的阵列在经过多次用蛋白质变性溶液再生后仍保留特异性 CTb 结合能力,并且在暴露于空气中后也保持稳定。此外,这些阵列在真空中稳定,这允许使用 MALDI-TOF 质谱法检测特异性结合的 CTb。这项工作证明了聚(脂质)双层阵列在高通量结合测定和脂质组学研究中的巨大潜力。