Lee I-Ning, Hosford Joseph, Wang Shuai, Hunt John A, Curran Judith M, Heath William P, Wong Lu Shin
Manchester Institute of Biotechnology & School of Chemistry, University of Manchester; School of Engineering, University of Liverpool.
Manchester Institute of Biotechnology & School of Chemistry, University of Manchester.
J Vis Exp. 2018 Jun 12(136):56967. doi: 10.3791/56967.
Scanning probe microscopy has enabled the creation of a variety of methods for the constructive ('additive') top-down fabrication of nanometer-scale features. Historically, a major drawback of scanning probe lithography has been the intrinsically low throughput of single probe systems. This has been tackled by the use of arrays of multiple probes to enable increased nanolithography throughput. In order to implement such parallelized nanolithography, the accurate alignment of probe arrays with the substrate surface is vital, so that all probes make contact with the surface simultaneously when lithographic patterning begins. This protocol describes the utilization of polymer pen lithography to produce nanometer-scale features over centimeter-sized areas, facilitated by the use of an algorithm for the rapid, accurate, and automated alignment of probe arrays. Here, nanolithography of thiols on gold substrates demonstrates the generation of features with high uniformity. These patterns are then functionalized with fibronectin for use in the context of surface-directed cell morphology studies.
扫描探针显微镜已促成了多种用于自上而下构建(“加法”)纳米级特征的方法的产生。从历史上看,扫描探针光刻技术的一个主要缺点是单探针系统的固有低通量。通过使用多个探针阵列来提高纳米光刻通量,这一问题已得到解决。为了实现这种并行纳米光刻,探针阵列与衬底表面的精确对准至关重要,以便在光刻图案化开始时所有探针能同时与表面接触。本方案描述了利用聚合物笔光刻技术在厘米级区域上制造纳米级特征,这借助了一种用于快速、准确和自动对准探针阵列的算法。在此,金基底上硫醇的纳米光刻展示了具有高均匀性的特征的生成。然后用纤连蛋白对这些图案进行功能化处理,以用于表面导向细胞形态学研究。