Chemistry and Physics of Interfaces, Department of Microsystems Engineering (IMTEK), University of Freiburg, Georges-Köhler-Allee 103, D-79110 Freiburg, Germany.
Langmuir. 2011 May 17;27(10):6116-23. doi: 10.1021/la1050833. Epub 2011 Apr 14.
For the miniaturization of biological assays, especially for the fabrication of microarrays, immobilization of biomolecules at the surfaces of the chips is the decisive factor. Accordingly, a variety of binding techniques have been developed over the years to immobilize DNA or proteins onto such substrates. Most of them require rather complex fabrication processes and sophisticated surface chemistry. Here, a comparatively simple immobilization technique is presented, which is based on the local generation of small spots of surface attached polymer networks. Immobilization is achieved in a one-step procedure: probe molecules are mixed with a photoactive copolymer in aqueous buffer, spotted onto a solid support, and cross-linked as well as bound to the substrate during brief flood exposure to UV light. The described procedure permits spatially confined surface functionalization and allows reliable binding of biological species to conventional substrates such as glass microscope slides as well as various types of plastic substrates with comparable performance. The latter also permits immobilization on structured, thermoformed substrates resulting in an all-plastic biochip platform, which is simple and cheap and seems to be promising for a variety of microdiagnostic applications.
为了实现生物分析的小型化,特别是微阵列的制造,生物分子在芯片表面的固定是决定性因素。因此,多年来已经开发了各种结合技术,将 DNA 或蛋白质固定到这些基底上。它们中的大多数需要相当复杂的制造工艺和复杂的表面化学。这里提出了一种相对简单的固定技术,该技术基于在表面附着聚合物网络的小斑点的局部生成。固定是通过一步程序实现的:将探针分子与光活性共聚物在水性缓冲液中混合,点样到固体载体上,并在短暂的紫外光照射下交联和结合到基底上。所描述的方法允许空间受限的表面功能化,并允许可靠地将生物物种结合到常规基底上,如玻璃显微镜载玻片以及各种类型的塑料基底,性能相当。后者还允许在结构化、热成型的基底上进行固定,从而形成全塑料生物芯片平台,该平台简单且廉价,似乎在各种微诊断应用中很有前景。