Department of Chemistry and Biochemistry, The University of Texas at Austin, Texas 78712, USA.
Small. 2012 Oct 22;8(20):3169-74. doi: 10.1002/smll.201200673. Epub 2012 Jul 16.
Protein molecules on solid surfaces are essential to a number of applications, such as biosensors, biomaterials, and drug delivery. In most approaches for protein immobilization, inter-molecular distances on the solid surface are not controlled and this may lead to aggregation and crowding. Here, a simple approach to immobilize individual protein molecules in a well-ordered 2D array is shown, using nanopatterns obtained from a polystyrene-block-poly(2-hydroxyethyl methacrylate) (PS-b-PHEMA) diblock copolymer thin film. This water-stable and protein-resistant polymer film contains hexagonally ordered PS cylindrical domains in a PHEMA matrix. The PS domains are activated by incorporating alkyne-functionalized PS and immobilizing azide-tagged proteins specifically onto each PS domain using "Click" chemistry. The nanometer size of the PS domain dictates that each domain can accommodate no more than one protein molecule, as verified by atomic force microscopy imaging. Immunoassay shows that the amount of specifically bound antibody scales with the number density of individual protein molecules on the 2D nanoarrays.
固体表面上的蛋白质分子对于许多应用至关重要,例如生物传感器、生物材料和药物输送。在大多数蛋白质固定化方法中,固体表面上的分子间距离不受控制,这可能导致聚集和拥挤。在这里,展示了一种使用聚苯乙烯嵌段聚(2-羟乙基甲基丙烯酸酯)(PS-b-PHEMA)嵌段共聚物薄膜获得的纳米图案,将单个蛋白质分子固定在有序的二维阵列中的简单方法。这种水稳定且抗蛋白质的聚合物膜在 PHEMA 基质中包含六方有序的 PS 圆柱畴。通过掺入炔基功能化的 PS 并使用“点击”化学将叠氮标记的蛋白质特异性地固定在每个 PS 畴上来激活 PS 畴。PS 畴的纳米尺寸决定了每个畴只能容纳不超过一个蛋白质分子,这通过原子力显微镜成像得到了验证。免疫测定表明,特异性结合的抗体量与二维纳米阵列上单个蛋白质分子的数量密度成正比。