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Photo‐electrochemical Bioanalysis of Guanosine Monophosphate Using Coupled Enzymatic Reactions at a CdS/ZnS Quantum Dot Electrode
34
Citations
33
References
2015
Year
EngineeringInorganic PhotochemistryBioelectrochemistryMolecular BiologyPhoto-electrochemical CellPhoto‐electrochemical BioanalysisChemistryRedox BiologyPhotoelectrochemistryChemical EngineeringBioenergeticsBioanalysisPhotocatalysisElectrode Reaction MechanismPhotochemistryBiochemistryMolecular ElectrochemistryBiocatalysisAdenosine TriphosphateCds/zns Quantum DotElectrochemistryCellular EnzymologyNatural SciencesLactate DehydrogenaseBioelectronicsEnzyme CatalysisElectroanalytical Sensor
A photo-electrochemical sensor for the specific detection of guanosine monophosphate (GMP) is demonstrated, based on three enzymes combined in a coupled reaction assay. The first reaction involves the adenosine triphosphate (ATP)-dependent conversion of GMP to guanosine diphosphate (GDP) by guanylate kinase, which warrants substrate specificity. The reaction products ADP and GDPare co-substrates for the enzymatic conversion of phosphoenolpyruvate to pyruvate in a second reaction mediated by pyruvate kinase. Pyruvate in turn is the co-substrate for lactate dehydrogenase that generates lactate via oxidation of nicotinamide adenine dinucleotide (reduced form) NADH to NAD(+). This third enzymatic reaction is electrochemically detected. For this purpose a CdS/ZnS quantum dot (QD) electrode is illuminated and the photocurrent response under fixed potential conditions is evaluated. The sequential enzyme reactions are first evaluated in solution. Subsequently, a sensor for GMP is constructed using polyelectrolytes for enzyme immobilization.
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