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Superoxide determination using membrane-engineered cells: An example of a novel concept for the construction of cell sensors with customized target recognition properties

[PDF] Sens act B chem superoxide determination.pdf (593.9Kb)
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URI: https://hdl.handle.net/10481/96197
DOI: 10.1016/J.SNB.2011.12.056
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Author
Moschopoulou, Georgia; Valero Griñán, María Teresa; Kintzios, Spyridon
Editorial
Elsevier
Materia
Bioelectric recognition assay
 
Cell biosensors
 
Immobilization
 
Membrane engineering
 
Superoxide dismutase
 
Superoxide ion
 
Date
2011
Referencia bibliográfica
Published version: Moschopoulou, Georgia et al. Superoxide determination using membrane-engineered cells: An example of a novel concept for the construction of cell sensors with customized target recognition properties. Sensors and Actuators B: Chemical Volume 175, December 2012, Pages 78-84. https://doi.org/10.1016/j.snb.2011.12.056
Sponsorship
EU Marie-Curie Research Training Network MRTN-CT-2006-035854
Abstract
Membrane-engineering is a generic methodology for increasing the selectivity of a cell biosensor against a target molecule, by electroinserting target-specific receptor molecules on the cell surface. We have previously reported the construction of an ultra-sensitive superoxide anion (O2−) sensor based on immobilized cells, which have been membrane-engineered with superoxide dismutase (SOD). In the present study, we provide evidence that superoxide dismutation triggered changes to the membrane potential of membrane-engineered fibroblast cells, as confirmed by electrophysiological and fluorescence assays. These changes were associated with changes in [Ca2+] , as revealed by the selective inhibition of intracellular calcium ion traffic. In addition, by conducting selective inhibition assays, we show that electroinserted SOD molecules retained their characteristic catalytic properties. We also investigated the effect of the concentration of electroinserted SOD molecules on the performance of the superoxide assay. Finally, we increased the sensitivity of the sensor by hundredfold to a detection limit of 1 pM O2− by changing the concentration of immobilized cells on the performance of the biosensor.
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