Interdisciplinary Nanoscience Center (iNANO) and ‡Department of Molecular Biology and Genetics, Aarhus University , Denmark.
J Phys Chem B. 2013 Sep 12;117(36):10376-83. doi: 10.1021/jp4038528. Epub 2013 Aug 28.
This paper presents the use of the quartz crystal microbalance with dissipation (QCM-D) combined with surface plasmon resonance (SPR) to probe protein adsorption at nanopatterned surfaces. Three different types of adsorbing materials, representing rigid discrete nanoparticles, dense protein films, and soft low density films have been studied on systematic varied circular nanostructures in the 100-1000 nm size range. Analysis and quantification of the QCM-D response from larger nanostructures could be understood and quantified in the same way as for homogeneous surfaces, while that for nanostructures of 100 and 200 nm diameter was significantly underestimated. Our findings suggest a size limitation of those techniques in analysis of adsorption at nanofeatures.
本文提出了将石英晶体微天平与耗散(QCM-D)结合表面等离子体共振(SPR)技术应用于探测纳米图案表面上的蛋白质吸附。研究了三种不同类型的吸附材料,分别代表刚性离散纳米粒子、致密蛋白质膜和软低密度膜,在 100-1000nm 尺寸范围内的系统变化的圆形纳米结构上进行了研究。对较大纳米结构的 QCM-D 响应的分析和量化可以与均匀表面的分析和量化一样理解和量化,而对于直径为 100nm 和 200nm 的纳米结构的分析则明显低估。我们的研究结果表明,这些技术在分析纳米特征吸附时存在尺寸限制。