Issue 12, 2011
From the journal:

Chemical Communications

Redox strategy for reversible attachment of biomolecules using bifunctional linkers†

Galina V. Dubacheva,*a   Mathieu Galibert,a   Liliane Coche-Guerente,a   Pascal Dumy,a   Didier Boturyna  and  Pierre Labbé*a  

* Corresponding authors

a Département de Chimie Moléculaire, UMR CNRS 5250, Université Joseph Fourier, ICMG FR CNRS 2607, BP53, 38041 Grenoble cedex 9, France
E-mail: galina.dubacheva@ujf-grenoble.fr, pierre.labbe@ujf-grenoble.fr
Fax: +33 456 520 805
Tel: +33 456 520 813

Abstract

Soft attachment of streptavidin to β-cyclodextrin-modified pegylated SAMs was efficiently performed in a reversible and repetitive way via orthogonal bifunctional linkers involving streptavidin–biotin recognition and redox-driven multivalent host–guest (β-cyclodextrin–ferrocene) interactions.

Graphical abstract: Redox strategy for reversible attachment of biomolecules using bifunctional linkers

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Article information

DOI
https://doi.org/10.1039/C0CC05647B
Article type
Communication
Submitted
17 Dec 2010
Accepted
27 Jan 2011
First published
15 Feb 2011

Chem. Commun., 2011,47, 3565-3567

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Redox strategy for reversible attachment of biomolecules using bifunctional linkers

G. V. Dubacheva, M. Galibert, L. Coche-Guerente, P. Dumy, D. Boturyn and P. Labbé, Chem. Commun., 2011, 47, 3565 DOI: 10.1039/C0CC05647B

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