Dynamic tracking of pathogenic receptor expression with live cells is made possible by pyrenyl glycoanthraquinones decorated on graphene electrodes.

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BackgroundConstruction of electrochemical impedance sensors by the self-assembly technique has become a promising strategy for the ‘label-free’ detection of protein-ligand interactions. However, previous impedance sensors are devoid of an inherent electrochemical signal, which limits the standardization of the sensors for protein recognition in a reproducible manner.ResultsWe designed and synthesized an anthraquinonyl glycoside (AG) where the anthraquinone (AQ) moiety can bind to the surface of a graphene-based working electrode while the glycoside serving as a ligand for lectin. By measuring the inherent voltammetric signal of AQ, the glycosides decorated on the working electrode could be simply quantified to obtain electrodes with a unified signal window. Subsequently, impedance analysis showed that the ‘standardized’ electrodes gave a reproducible electrochemical response to a selective lectin with no signal variation in the presence of unselective proteins.ConclusionAnthraquinone-modified ligands could be used to facilitate the standardization of electrochemical impedance sensors for the reproducible, selective analysis of ligand-protein interactions.Electronic supplementary materialThe online version of this article (doi:10.1186/s13065-014-0067-y) contains supplementary material, which is available to authorized users.

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