Department of Biological, Chemical and Physical Sciences, Illinois Institute of Technology, Chicago, Illinois 60616, United States.
Langmuir. 2012 Jan 10;28(1):548-56. doi: 10.1021/la202053k. Epub 2011 Dec 6.
We report a robust strategy for conjugating mixtures of two or more protein domains to nonfouling polyurethane surfaces. In our strategy, the carbamate groups of polyurethane are reacted with zirconium alkoxide from the vapor phase to give a surface-bound oxide that serves as a chemical layer that can be used to bond organics to the polymer substrate. A hydroxyalkylphosphonate monolayer was synthesized on this layer, which was then used to covalently bind primary amine groups in protein domains using chloroformate-derived cross-linking. The effectiveness of this synthesis strategy was gauged by using an ELISA to measure competitive, covalent bonding of cell-binding (III(9-10)) and fibronectin-binding (III(1-2)) domains of the cell adhesion protein fibronectin. Cell adhesion, spreading, and fibronectin matrix assembly were examined on surfaces conjugated with single domains, a 1:1 surface mixture of III(1-2) and III(9-10), and a recombinant protein "duplex" containing both domains in one fusion protein. The mixture performed as well as or better than the other surfaces in these assays. Our surface activation strategy is amenable to a wide range of polymer substrates and free amino group-containing protein fragments. As such, this technique may be used to create biologically specific materials through the immobilization of specific protein groups or mixtures thereof on a substrate surface.
我们报告了一种将两种或多种蛋白质结构域混合偶联到非粘性聚氨酯表面的稳健策略。在我们的策略中,聚氨酯的氨基甲酸酯基团与来自气相的锆烷醇盐反应,得到表面结合的氧化物,作为化学层,可用于将有机物键合到聚合物基底上。在该层上合成了羟烷基膦酸盐单层,然后使用氯甲酸酯衍生的交联剂将其共价键合到蛋白质结构域中的伯胺基团上。通过使用 ELISA 测量细胞结合(III(9-10))和纤连蛋白结合(III(1-2))结构域的竞争、共价键合,来评估这种合成策略的有效性。纤连蛋白的细胞粘附蛋白。在与单个结构域、III(1-2)和 III(9-10)的 1:1 表面混合物以及含有两个结构域的重组蛋白“双链体”偶联的表面上检查了细胞粘附、铺展和纤连蛋白基质组装。在这些测定中,混合物的性能与其他表面一样好或更好。我们的表面激活策略适用于多种聚合物基底和含有游离氨基基团的蛋白质片段。因此,该技术可通过将特定蛋白质基团或其混合物固定在基底表面上来创建具有生物特异性的材料。