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Peptides for the Biofunctionalization of Silicon for Use in Optical Sensing with Porous Silicon Microcavities
Authors:Elias Estephan  Marie‐Belle Saab  Vivechana Agarwal  Frédéric J G Cuisinier  Christian Larroque  Csilla Gergely
Affiliation:1. EA 4203, UFR Odontologie, Université Montpellier 1, 34193 Montpellier Cedex 5, France, Laboratoire Charles Coulomb, UMR 5221 CNRS‐Université Montpellier 2, 34095, Montpellier Cedex 5, France;2. Laboratoire Charles Coulomb, UMR 5221, CNRS‐Université Montpellier 1, 34095, Montpellier Cedex 5, France;3. CIICAP‐ Universidad Autonoma del Estado de Morelos, Av. Universidad 1001, Col Chamilpa, Cuernavaca, Mor., México;4. EA 4203, UFR Odontologie, Université Montpellier 1, 34193 Montpellier Cedex 5, France;5. IRCM/INSERM896, Centre Régional de Lutte contre le Cancer Val d’Aurelle – Paul Lamarque, Université Montpellier 1, 34298 Montpellier, France;6. Laboratoire Charles Coulomb, UMR 5221 CNRS‐Université Montpellier 2, 34095, Montpellier Cedex 5, France
Abstract:Addressing the surface chemistry of silicon is of fundamental scientific and technical significance due to the wide use of this material in electronics and optics. A novel method of functionalizing silicon (Si) via short peptides with binding specificity for Si is presented. The peptide presenting the highest affinity for Si is identified via phage display technology, and the 12‐mer LLADTTHHRPWT and SPGLSLVSHMQT peptides were found to be specific for the n+‐Si and p+‐Si surfaces, respectively. In our sensing application, the obtained peptides are used as functionalizing linkers to allow porous silicon microcavities to bind biotin and then capture streptavidin. Molecular detection is monitored via reflectometric interference spectra as shifts in the resonance peaks of the cavity structure. An improved streptavidin sensing (21 times lower detection limit) with peptide‐functionalized porous silicon microcavities is demonstrated, compared to sensing performed with devices functionalized with the commonly used silanization method, suggesting that the modification of Si via Si‐specific peptides provides better interface layers for molecular detection. High‐resolution atomic force microscopy images corroborate this result and reveal the formation of ordered nanometer‐sized molecular layers when peptide‐route functionalization is performed.
Keywords:phage display  porous silicon  functionalization  peptides  biosensing
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