Department of Chemistry and Center for Materials Innovation, Washington University in St. Louis, St. Louis, Missouri 63130, USA.
Langmuir. 2012 Nov 27;28(47):16237-42. doi: 10.1021/la303429a. Epub 2012 Nov 14.
This work investigates self-assembled monolayers that were formed from a glycol-terminated thiol monomer and were patterned using photoinduced monolayer desorption. Utilizing direct-write photolithography provided a facile means to generate complex protein patterns containing gradients and punctate regions. The ablated glycol monolayers were characterized using scanning probe microscopy, which allowed us to observe differences in the nanomechanical properties between the patterned and nonpatterned regions of the substrate. The patterned regions on the surface adsorbed proteins, and this process was monitored quantitatively using surface plasmon resonance imaging (SPRi). Moreover, the concentration of the protein could be controlled accurately by simply setting the gray level in the 8-bit image. Adsorbed protein was probed using a commercially available antibody binding assay, which showed significant enhancement over the background. The ability to produce complex protein patterns will contribute greatly to creating in vitro models that more accurately mimic an in vivo environment.
这项工作研究了自组装单分子层,该单分子层是由末端带有二醇的硫醇单体形成的,并通过光诱导单层脱附进行图案化。利用直写光刻技术,提供了一种简便的方法来生成含有梯度和点状区域的复杂蛋白质图案。使用扫描探针显微镜对烧蚀的二醇单层进行了表征,这使我们能够观察到基底的图案化和非图案化区域之间纳米力学性能的差异。表面的图案化区域吸附蛋白质,并且可以使用表面等离子体共振成像(SPRi)定量监测该过程。此外,通过简单地设置 8 位图像中的灰度级,就可以准确控制蛋白质的浓度。使用商业上可用的抗体结合测定法探测吸附的蛋白质,结果表明其显著高于背景。产生复杂蛋白质图案的能力将极大地有助于创建更准确模拟体内环境的体外模型。