Segerer Felix Jakob, Röttgermann Peter Johan Friedrich, Schuster Simon, Piera Alberola Alicia, Zahler Stefan, Rädler Joachim Oskar
Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Geschwister-Scholl-Platz 1, D-80539 Munich, Germany.
Department of Pharmacy - Center for Drug Research, Pharmaceutical Biology, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, D-81377 Munich, Germany.
Biointerphases. 2016 Mar 22;11(1):011005. doi: 10.1116/1.4940703.
Micropatterning techniques have become an important tool for the study of cell behavior in controlled microenvironments. As a consequence, several approaches for the creation of micropatterns have been developed in recent years. However, the diversity of substrates, coatings, and complex patterns used in cell science is so great that no single existing technique is capable of fabricating designs suitable for all experimental conditions. Hence, there is a need for patterning protocols that are flexible with regard to the materials used and compatible with different patterning strategies to create more elaborate setups. In this work, the authors present a versatile approach to micropatterning. The protocol is based on plasma treatment, protein coating, and a poly(L-lysine)-grafted-poly(ethylene glycol) backfill step, and produces homogeneous patterns on a variety of substrates. Protein density within the patterns can be controlled, and density gradients of surface-bound protein can be formed. Moreover, by combining the method with microcontact printing, it is possible to generate patterns composed of three different components within one iteration of the protocol. The technique is simple to implement and should enable cell science labs to create a broad range of complex and highly specialized microenvironments.
微图案化技术已成为研究细胞在可控微环境中行为的重要工具。因此,近年来已开发出多种创建微图案的方法。然而,细胞科学中使用的底物、涂层和复杂图案的多样性非常大,以至于现有的单一技术都无法制造出适用于所有实验条件的设计。因此,需要在所用材料方面具有灵活性且与不同图案化策略兼容的图案化方案,以创建更精细的设置。在这项工作中,作者提出了一种通用的微图案化方法。该方案基于等离子体处理、蛋白质涂层和聚(L-赖氨酸)接枝聚(乙二醇)回填步骤,并在各种底物上产生均匀的图案。图案内的蛋白质密度可以控制,并且可以形成表面结合蛋白质的密度梯度。此外,通过将该方法与微接触印刷相结合,有可能在该方案的一次迭代中生成由三种不同成分组成的图案。该技术易于实施,应该能够使细胞科学实验室创建广泛的复杂且高度专业化的微环境。