In this contribution we report on our recent studies on peptide-based self-assembled monolayers (SAMs). We show that helical oligopeptides formed by Cα-tetrasubstituted Cα-amino acids can form stable and densely-packed nanometric films on a gold surface. Three issues will be discussed: I) the morphology of peptide thiol SAMs on a gold surface, II) the electron transfer properties of peptide SAMs functionalized with electro- or photoactive probes, and III) the versatility of helical peptide building blocks in the engineering of complex nanostructures. These findings will pave the way for feasible applications in the fields of electrochemical sensing, molecular electronics, and bionanotechnology.

Gatto, E., Formaggio, F., Toniolo, C., Venanzi, M. (2013). Self-Assembled Monolayers formed by Conformationally Constrained Oligopeptides. CHIMICA OGGI-CHEMISTRY TODAY, 31, 2-6.

Self-Assembled Monolayers formed by Conformationally Constrained Oligopeptides.

GATTO, EMANUELA;VENANZI, MARIANO
2013-01-01

Abstract

In this contribution we report on our recent studies on peptide-based self-assembled monolayers (SAMs). We show that helical oligopeptides formed by Cα-tetrasubstituted Cα-amino acids can form stable and densely-packed nanometric films on a gold surface. Three issues will be discussed: I) the morphology of peptide thiol SAMs on a gold surface, II) the electron transfer properties of peptide SAMs functionalized with electro- or photoactive probes, and III) the versatility of helical peptide building blocks in the engineering of complex nanostructures. These findings will pave the way for feasible applications in the fields of electrochemical sensing, molecular electronics, and bionanotechnology.
2013
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/02 - CHIMICA FISICA
English
peptide self-assembled monolayers; c -tetrasubstituted amino acids; electron transfer; photocurrent generation
Gatto, E., Formaggio, F., Toniolo, C., Venanzi, M. (2013). Self-Assembled Monolayers formed by Conformationally Constrained Oligopeptides. CHIMICA OGGI-CHEMISTRY TODAY, 31, 2-6.
Gatto, E; Formaggio, F; Toniolo, C; Venanzi, M
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/79472
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