Solano Ilaria, Parisse Pietro, Cavalleri Ornella, Gramazio Federico, Casalis Loredana, Canepa Maurizio
Dipartimento di Fisica, Università di Genova, Via Dodecaneso 33, Genova, Italy.
Elettra Sincrotrone Trieste S.C.p.A., s.s. 14 km 163,5 in Area Science Park, Basovizza, Trieste, Italy.
Beilstein J Nanotechnol. 2016 Apr 13;7:544-53. doi: 10.3762/bjnano.7.48. eCollection 2016.
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.
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).
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 δΔ i +1 ,i (λ), δΨ i +1 ,i (λ) (layer-addition mode) and δΔ(†) i ', i +1(λ), δΨ(†) i ', 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.
生物芯片中一种通用的蛋白质 - 表面偶联策略利用了负载Ni(II)的次氮基三乙酸(NTA)基团对多组氨酸的亲和力。基于光学反射率测量的方法,如光谱椭偏仪(SE),能够对表面分子的吸附/解吸进行无标记、非侵入性监测。
本文描述了一项关于六组氨酸(His6)在带有NTA端基的硫醇盐自组装单层功能化金基底上相互作用的SE研究。通过系统地应用差异光谱法,该方法强调了分子膜在纳米尺度增厚/减薄时椭偏光谱响应的微小变化,我们表征了该过程的不同步骤,如金的NTA功能化、His6层的吸附以及与竞争性配体反应后其最终的置换。这些薄膜在液体中以及在环境空气中进行了非原位研究。SE研究得到了基于纳米光刻方法(纳米接枝模式)的原子力显微镜测量的补充。
我们处理SE数据所采用的方法,利用了该方法的全部光谱潜力和基本光学模型,能够呈现出整个过程中膜厚度的变化情况。δΔ({i + 1,i})(λ)、δΨ({i + 1,i})(λ)(层添加模式)和δΔ(^{(\dagger)}{i',i + 1})(λ)、δΨ(^{(\dagger)}{i',i + + + 1})(λ)(层去除模式)差异光谱的结合,使我们能够清楚地区分由于非特异性相互作用导致的His6在无镍NTA层上的吸附,与由NTA自组装单分子层负载Ni(II)诱导形成的更厚的His6整齐膜的形成。