Abstract
Protein biochips are miniaturized biological sensors intended to analyze and characterize biomolecule interactions with high throughput. An important issue when developing such biochips is substrate passivation. The support is rendered inert in order to avoid non-specific adsorption. Strategic control of the non-specific protein adsorption can be achieved by creating a resistant self-assembled monolayer (SAM) based on polyethylene glycol (PEG). The degree of resistance depends on the PEG surface density, i.e. the number of PEG units the molecule contains. Infrared-visible sum-frequency generation (SFG) spectroscopy (Lambert et al., Appl Spectrosc Rev 40:103–145, 2005) is used to in-vestigate the vibrational fingerprint of a PEG self-assembled monolayer adsorbed on a flat platinum surface, in the 2,750–3,050 cm−1 frequency range. The objec-tive is to characterize the SFG baseline of the biosensor that will be further developed by mixing the PEG antifouling layer with bioactive host molecules. Nanostructures will then be implemented on the substrate in order to enhance the SFG signal through localized surface plasmon resonances (Lis et al., Adv Opt Mater 1:244–255, 2013). The ultimate goal will be to detect the SFG signature of the antigen/antibody recognition process at the interface of the above biosensing layer.
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Peerboom, N. et al. (2015). Characterization of Polyethylene Glycol Self-Assembled Monolayers by Means of Sum-Frequency Generation Spectroscopy for Biosensor Applications. In: Di Bartolo, B., Collins, J., Silvestri, L. (eds) Nano-Structures for Optics and Photonics. NATO Science for Peace and Security Series B: Physics and Biophysics. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-9133-5_62
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DOI: https://doi.org/10.1007/978-94-017-9133-5_62
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Publisher Name: Springer, Dordrecht
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Online ISBN: 978-94-017-9133-5
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