School of Life Science and Biotechnology, Dalian University of Technology, No. 2 Linggong Road, Dalian 116023, PR China.
ACS Appl Mater Interfaces. 2013 Jan 23;5(2):386-94. doi: 10.1021/am3024355. Epub 2012 Dec 31.
Optical biosensing techniques have become of key importance for label-free monitoring of biomolecular interactions in the current proteomics era. Together with an increasing emphasis on high-throughput applications in functional proteomics and drug discovery, there has been demand for facile and generally applicable methods for the immobilization of a wide range of receptor proteins. Here, we developed a polymer platform for microring resonator biosensors, which allows the immobilization of receptor proteins on the surface of waveguide directly without any additional modification. A sol-gel process based on a mixture of three precursors was employed to prepare a liquid hybrid polysiloxane, which was photopatternable for the photocuring process and UV imprint. Waveguide films were prepared on silicon substrates by spin coating and characterized by atomic force microscopy for roughness, and protein adsorption. The results showed that the surface of the polymer film was smooth (rms = 0.658 nm), and exhibited a moderate hydrophobicity with the water contact angle of 97°. Such a hydrophobic extent could provide a necessary binding strength for stable immobilization of proteins on the material surface in various sensing conditions. Biological activity of the immobilized Staphylococcal protein A and its corresponding biosensing performance were demonstrated by its specific recognition of human Immunoglobulin G. This study showed the potential of preparing dense, homogeneous, specific, and stable biosensing surfaces by immobilizing receptor proteins on polymer-based optical devices through the direct physical adsorption method. We expect that such polymer waveguide could be of special interest in developing low-cost and robust optical biosensing platform for multidimensional arrays.
光学生物传感技术在当前蛋白质组学时代对于无标记监测生物分子相互作用变得至关重要。随着在功能蛋白质组学和药物发现中对高通量应用的重视程度不断提高,人们对简便且通用的方法的需求也在不断增加,这种方法可用于固定广泛的受体蛋白。在这里,我们为微环谐振器生物传感器开发了一种聚合物平台,该平台允许将受体蛋白直接固定在波导表面上,而无需进行任何其他修饰。采用基于三种前体混合物的溶胶-凝胶工艺来制备液体杂化聚硅氧烷,该液体杂化聚硅氧烷可通过光固化过程和 UV 压印进行光图案化。通过旋涂法在硅衬底上制备波导膜,并通过原子力显微镜对粗糙度和蛋白质吸附进行了表征。结果表明,聚合物膜的表面光滑(均方根=0.658nm),并且具有适度的疏水性,水接触角为 97°。这种疏水性程度可以为在各种传感条件下在材料表面上稳定固定蛋白质提供必要的结合强度。通过固定化金黄色葡萄球菌蛋白 A 及其相应的生物传感性能,证明了其对人免疫球蛋白 G 的特异性识别。这项研究表明,通过直接物理吸附方法将受体蛋白固定在基于聚合物的光学器件上,可以制备致密、均匀、特异和稳定的生物传感表面,具有很大的潜力。我们期望这种聚合物波导在开发低成本、稳健的多维阵列光学生物传感平台方面具有特殊的应用前景。