Ducker Robert E, Janusz Stefan, Sun Shuqing, Leggett Graham J
Department of Chemistry, University of Sheffield, Brook Hill, Sheffield S3 7HF, United Kingdom.
J Am Chem Soc. 2007 Dec 5;129(48):14842-3. doi: 10.1021/ja0749800. Epub 2007 Nov 8.
Exposure of oligo(ethylene glycol) (OEG)-terminated self-assembled monolayers (SAMs) to UV light leads to the formation of aldehyde groups, leading to a simple one-step method for the introduction of reactive functional groups to protein-resistant surfaces. X-ray photoelectron spectroscopy has been used to demonstrate binding of amines to the modified surfaces, while surface plasmon resonance has shown that proteins are covalently bound. Modified OEG monolayers bind streptavidin at least as well as N-hydroxysuccinimidyl ester functionalized monolayers. Micrometer and nanometer-scale patterns are conveniently fabricated by exposing the monolayers using, respectively, a mask and a scanning near-field optical microscope.
将以低聚乙二醇(OEG)为端基的自组装单分子层(SAMs)暴露于紫外光下会导致醛基的形成,从而产生一种将反应性官能团引入抗蛋白质表面的简单一步法。X射线光电子能谱已被用于证明胺与修饰表面的结合,而表面等离子体共振表明蛋白质是共价结合的。修饰后的OEG单分子层结合链霉亲和素的能力至少与N-羟基琥珀酰亚胺酯功能化单分子层相当。通过分别使用掩膜和扫描近场光学显微镜对单分子层进行曝光,可以方便地制备微米级和纳米级图案。