Langmuir, 24 (6), 2878 -2883, 2008. 10.1021/la703536a S0743-7463(70)03536-9
Web Release Date: February 1, 2008

Copyright © 2008 American Chemical Society

Electrochemical Rectification by Redox-Labeled Bioconjugates: Molecular Building Blocks for the Construction of Biodiodes

Omar Azzaroni,* Mnica Mir, Marta lvarez, Louis Tiefenauer, and Wolfgang Knoll

Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128, Mainz, Germany, and Life Sciences Department, Paul Scherrer Institute, CH 5232 PSI, Villigen, Switzerland

Received November 13, 2007

In Final Form: December 2, 2007

Abstract:

In the present work, we describe the properties of a bifunctional redox-labeled bioconjugate at electrode surfaces mediating the electron transfer across the electrode-electrolyte interface. We show that the assembly of ferrocene-labeled streptavidin on biotinylated electrodes results in a reproducible unidirectional current flow in the presence of electron donors in solution. Such rectifying films were built up by spontaneous binding of tetrameric streptavidin molecules to biotin centers immobilized on the electrode surface. Due to the high affinitiy of biotin to streptavidin, such bifunctional films completely bind any biotinylated compounds. The charge transport between donors in solution and the Au electrode is mediated by the ferrocene moieties, allowing us to develop a molecular rectifier. Our experimental results suggest that such redox-labeled proteins with a high binding capacity constitute a promising alternative to organic compounds used in molecular electronics.


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