AG Roth-Lab for Microarray Copying, ZBSA-Centre for Biological Systems Analysis, University of Freiburg, Habsburgerstrasse 49, 79104, Freiburg, Germany.
Faculty of Biology, Biology 3, University of Freiburg, Schänzlestrasse 1, 79104, Freiburg, Germany.
Chembiochem. 2019 Jun 14;20(12):1554-1562. doi: 10.1002/cbic.201800699. Epub 2019 Apr 25.
Protein microarrays are essential to understand complex protein interaction networks. Their production, however, is a challenge and renders this technology unattractive for many laboratories. Recent developments in cell-free protein microarray generation offer new opportunities, but are still expensive and cumbersome in practice. Herein, we describe a cost-effective and user-friendly method for the cell-free production of protein microarrays. From a polydimethylsiloxane (PDMS) flow cell containing an expressible DNA microarray, proteins of interest are synthesised by cell-free expression and then immobilised on a capture surface. The resulting protein microarray can be regarded as a "copy" of the DNA microarray. 2 His - and Halo-tagged fluorescent reference proteins were used to demonstrate the functionality of nickel nitrilotriacetic acid (Ni-NTA) and Halo-bind surfaces in this copy system. The described process can be repeated several times on the same DNA microarray. The identity and functionality of the proteins were proven during the copy process by their fluorescence and on the surface through a fluorescent immune assay. Also, single-colour reflectometry (SCORE) was applied to show that, on such copied arrays, real-time binding kinetic measurements were possible.
蛋白质微阵列对于理解复杂的蛋白质相互作用网络至关重要。然而,它们的生产是一个挑战,使得这项技术对许多实验室来说没有吸引力。最近在无细胞蛋白质微阵列生成方面的发展提供了新的机会,但在实践中仍然昂贵且繁琐。在此,我们描述了一种用于无细胞生产蛋白质微阵列的经济高效且用户友好的方法。从含有可表达 DNA 微阵列的聚二甲基硅氧烷 (PDMS) 流控芯片中,通过无细胞表达合成感兴趣的蛋白质,然后将其固定在捕获表面上。由此产生的蛋白质微阵列可以被视为 DNA 微阵列的“副本”。2His 和 Halo 标记的荧光参考蛋白被用于证明镍氮三乙酸 (Ni-NTA) 和 Halo 结合表面在该复制系统中的功能。可以在同一个 DNA 微阵列上重复该过程多次。在复制过程中,通过它们的荧光和在表面上的荧光免疫测定来证明蛋白质的身份和功能。此外,还应用单波长反射光度法 (SCORE) 表明,在这种复制的阵列上,可以进行实时结合动力学测量。