Issue 12, 2011

Redox strategy for reversible attachment of biomolecules using bifunctional linkers

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

Supplementary files

Article information

Article type
Communication
Submitted
17 Dec 2010
Accepted
27 Jan 2011
First published
15 Feb 2011

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

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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