Jun Yongseok, Cha Taewoon, Guo Athena, Zhu X-Y
Department of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis, MN 55455ZHU, USA.
Biomaterials. 2004 Aug;25(17):3503-9. doi: 10.1016/j.biomaterials.2003.10.053.
We demonstrate spatially localized immobilization of protein molecules on high-density poly(ethylene glycol) (PEG) coated Si(111). Patterns of HO- and CH3O-terminated PEG regions are formed on silicon surfaces based on soft lithography techniques and an efficient reaction between alcohol functional groups and chlorine-terminated silicon. Activation of the HO-terminated PEG brush is achieved via either partial oxidation to form aldehyde groups or via attachment of efficient leaving groups. Protein molecules are covalently immobilized to these activated regions on the PEG/Si surface.
我们展示了蛋白质分子在高密度聚乙二醇(PEG)包覆的Si(111)上的空间定位固定。基于软光刻技术以及醇官能团与氯端基硅之间的有效反应,在硅表面形成了羟基和甲氧基封端的PEG区域图案。通过部分氧化形成醛基或连接有效的离去基团来实现羟基封端的PEG刷的活化。蛋白质分子被共价固定在PEG/Si表面的这些活化区域上。