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Investigating organic multilayers by spectroscopic ellipsometry: Specific and non-specific interactions of polyhistidine with NTA self-assembled monolayers

机译:通过光谱椭圆偏振法研究有机多层:聚组氨酸与NTA自组装单层的特异性和非特异性相互作用

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摘要

Background: A versatile strategy for protein-surface coupling in biochips exploits the affinity for polyhistidine of the nitrilotriacetic acid (NTA) group loaded with Ni(II). Methods based on optical reflectivity measurements such as spectroscopic ellipsometry (SE) allow for label-free, non-invasive monitoring of molecule adsorption/desorption at surfaces. Results: This paper describes a SE study about the interaction of hexahistidine (His6) on gold substrates functionalized with a thiolate self-assembled monolayer bearing the NTA end group. By systematically applying the difference spectra method, which emphasizes the small changes of the ellipsometry spectral response upon the nanoscale thickening/thinning of the molecular film, we characterized different steps of the process such as the NTA-functionalization of Au, the adsorption of the His6 layer and its eventual displacement after reaction with competitive ligands. The films were investigated in liquid, and ex situ in ambient air. The SE investigation has been complemented by AFM measurements based on nanolithography methods (nanografting mode). Conclusion: Our approach to the SE data, exploiting the full spectroscopic potential of the method and basic optical models, was able to provide a picture of the variation of the film thickness along the process. The combination of δΔi+1,i(λ), δΨi+1,i(λ) (layer-addition mode) and δΔi',i+1†(λ), δΨi',i+1†(λ) (layer-removal mode) difference spectra allowed us to clearly disentangle the adsorption of His6 on the Ni-free NTA layer, due to non specific interactions, from the formation of a neatly thicker His6 film induced by the Ni(II)-loading of the NTA SAM.
机译:背景:生物芯片中蛋白质-表面偶联的通用策略是利用负载Ni(II)的次氮基三乙酸(NTA)组对多组氨酸的亲和力。基于光反射率测量的方法(如椭圆偏振光谱法(SE))可实现对表面分子吸附/解吸的无标签,无创监测。结果:本文描述了关于六组氨酸(His6)在带有NTA端基的硫醇盐自组装单层功能化的金基质上的相互作用的SE研究。通过系统地应用差异光谱法,该方法强调了椭圆偏振光谱响应在分子膜的纳米级增厚/变薄上的微小变化,我们表征了该工艺的不同步骤,例如NTA官能化Au,His6的吸附层及其与竞争性配体反应后的最终位移。在液体中和在环境空气中非原位地研究膜。 SE研究得到了基于纳米光刻方法(纳米接枝模式)的AFM测量的补充。结论:我们利用SE方法的全部光谱潜力和基本光学模型对SE数据进行处理的方法能够提供整个过程中膜厚变化的图像。 δΔi+ 1,i(λ),δΨi+ 1,i(λ)(叠加层模式)和δΔi',i + 1†(λ),δΨi',i + 1†(λ)(层的组合) -去除模式)差异光谱使我们能够清楚地分辨出由于非特异性相互作用,His6在无镍NTA层上的吸附与NTA的Ni(II)加载诱导形成的整齐而厚的His6膜的形成有关。萨姆

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