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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A biomolecule friendly photolithographic process for fabrication of protein microarrays on polymeric films coated on silicon chips
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A biomolecule friendly photolithographic process for fabrication of protein microarrays on polymeric films coated on silicon chips

机译:生物分子友好的光刻工艺,用于在涂在硅芯片上的聚合物膜上制造蛋白质微阵列

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摘要

The last years, there is a steadily growing demand for methods and materials appropriate to create patterns of biomolecules for bioanalytical applications. Here, a photolithographic method for patterning biomolecules onto a silicon surface coated with a polymeric layer of high protein binding capacity is presented. The patterning process does not affect the polymeric film and the activity of the immobilized onto the surface biomolecules. Therefore, it permits sequential immobilization of different biomolecules on spatially distinct areas on the same solid support. The polymeric layer is based on a commercially available photoresist (AZ5214) that is cured at high temperature in order to provide a stable substrate for creation of protein microarrays by the developed photolithographic process. The photolithographic material consists of a (meth)acrylate copolymer and a sulfonium salt as a photoacid generator, and it is lithographically processed by thermal treatment at temperatures ≤50 °C, development with dilute aqueous basic developer solutions and exposure at wavelengths above 300 nm. Following this photolithographic procedure onto the polymeric layer coated silicon surface, protein spots with diameters ranging from 2 to 50 μm were created. The proposed methodology provided good intra-spot homogeneity (CV ≤5%) and inter-spot repeatability (CV ≤5%), as it was determined through epifluorescence microscopy after reaction of the immobilized proteins with their respective fluorescently labeled binding counterparts. Moreover, the polymeric film selected for immobilization of biomolecules presented high protein binding capacity, which was at least three folds higher than that obtained using aminosilanized surfaces. The proposed methodology is expected to facilitate considerably the fabrication of dense protein microarrays for bioanalytical applications.
机译:过去几年,对适于创建用于生物分析应用的生物分子模式的方法和材料的需求在稳步增长。在这里,提出了一种光刻方法,用于将生物分子图案化到涂有高蛋白质结合能力聚合物层的硅表面上。图案化过程不影响聚合物膜和固定在表面生物分子上的活性。因此,它允许将不同生物分子顺序固定在同一固体支持物的空间不同区域上。聚合物层基于可商购的光致抗蚀剂(AZ5214),该光致抗蚀剂在高温下进行固化,以提供稳定的底物,以通过开发的光刻工艺产生蛋白质微阵列。该光刻材料由(甲基)丙烯酸酯共聚物和作为光酸产生剂的sulf盐组成,并通过在≤50°C的温度下进行热处理,使用稀碱性显影剂水溶液显影并在300 nm以上的波长曝光进行光刻处理。在该光刻步骤之后,在涂覆有聚合物层的硅表面上,创建了直径范围为2至50μm的蛋白质斑点。所提出的方法提供了良好的斑点内均一性(CV≤5%)和斑点间可重复性(CV≤5%),因为固定化蛋白质与它们各自的荧光标记结合对应物反应后通过表面荧光显微镜确定。此外,选择用于固定生物分子的聚合物膜具有高蛋白结合能力,比使用氨基硅烷化表面获得的结合能力高至少三倍。预期所提出的方法将极大地促进用于生物分析应用的致密蛋白质微阵列的制造。

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