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

Abstract

Summary 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 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.

Morphological and Mechanical Characterization of DNA SAMs Combining Nanolithography with AFM and Optical Methods

“…For SE measurements on ultrathin organic films, in order to emphasize the film contribution to the SE data, we followed a difference spectra analysis method that has been previously applied to organic monolayers [ 40 , 47 , 48 ]. Therefore, cleaned Arrandee samples were first characterized in situ in TE buffer, subsequently incubated in the C 6 -ssDNA solution for 24 h, and then rinsed and characterized by SE in situ in TE buffer.…”