Issue 14, 2015

Encapsulated enzymes with integrated fluorescence-control of enzymatic activity

Abstract

A fluorescence-based particle sensor for oxaloacetic acid is presented. In the presence of nicotinamide adenine dinucleotide as a cofactor, oxaloacetic acid is converted by malate dehydrogenase into L-malic acid. The progress of the reaction is monitored by sensing of proton consumption with an integrated pH sensor. The kinetics of this sensor are investigated on a single particle level. This work demonstrates the feasibility to detect analytes upon their enzymatic conversion into a product, which in turn can be sensed with a fluorophore responding to changes in the concentration of this product. Integration of enzymes and fluorophores into one carrier particle, as demonstrated here for the case of polyelectrolyte polymer capsules, allows the range of analytes that can be detected with fluorescence to be extended, as it enhances selectivity. This coupled system allows enzymatic activity, as well as the kinetics of malate dehydrogenase, to be monitored.

Graphical abstract: Encapsulated enzymes with integrated fluorescence-control of enzymatic activity

Supplementary files

Article information

Article type
Paper
Submitted
16 Dec 2014
Accepted
16 Feb 2015
First published
18 Feb 2015
This article is Open Access
Creative Commons BY license

J. Mater. Chem. B, 2015,3, 2801-2807

Author version available

Encapsulated enzymes with integrated fluorescence-control of enzymatic activity

P. K. Harimech, R. Hartmann, J. Rejman, P. del Pino, P. Rivera-Gil and W. J. Parak, J. Mater. Chem. B, 2015, 3, 2801 DOI: 10.1039/C4TB02077D

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