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Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing

Here, we present a study on the incorporation and characterization of the enzyme alkaline phosphatase (ALP) into a three-dimensional polymeric network through a green protocol to obtain transparent hydrogels (ALP@AETA) that can be stored at room temperature and potentially used as a disposable biose...

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Autores principales: Alacid, Yolanda, Martínez-Tomé, María José, Esquembre, Rocío, Herrero, M. Antonia, Mateo, C. Reyes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917215/
https://www.ncbi.nlm.nih.gov/pubmed/36769007
http://dx.doi.org/10.3390/ijms24032672
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author Alacid, Yolanda
Martínez-Tomé, María José
Esquembre, Rocío
Herrero, M. Antonia
Mateo, C. Reyes
author_facet Alacid, Yolanda
Martínez-Tomé, María José
Esquembre, Rocío
Herrero, M. Antonia
Mateo, C. Reyes
author_sort Alacid, Yolanda
collection PubMed
description Here, we present a study on the incorporation and characterization of the enzyme alkaline phosphatase (ALP) into a three-dimensional polymeric network through a green protocol to obtain transparent hydrogels (ALP@AETA) that can be stored at room temperature and potentially used as a disposable biosensor platform for the rapid detection of ALP inhibitors. For this purpose, different strategies for the immobilization of ALP in the hydrogel were examined and the properties of the new material, compared to the hydrogel in the absence of enzyme, were studied. The conformation and stability of the immobilized enzyme were characterized by monitoring the changes in its intrinsic fluorescence as a function of temperature, in order to study the unfolding/folding process inside the hydrogel, inherently related to the enzyme activity. The results show that the immobilized enzyme retains its activity, slightly increases its thermal stability and can be stored as a xerogel at room temperature without losing its properties. A small portion of a few millimeters of ALP@AETA xerogel was sufficient to perform enzymatic activity inhibition assays, so as a proof of concept, the device was tested as a portable optical biosensor for the detection of phosphate in water with satisfactory results. Given the good stability of the ALP@AETA xerogel and the interesting applications of ALP, not only in the environmental field but also as a therapeutic enzyme, we believe that this study could be of great use for the development of new devices for sensing and protein delivery.
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spelling pubmed-99172152023-02-11 Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing Alacid, Yolanda Martínez-Tomé, María José Esquembre, Rocío Herrero, M. Antonia Mateo, C. Reyes Int J Mol Sci Article Here, we present a study on the incorporation and characterization of the enzyme alkaline phosphatase (ALP) into a three-dimensional polymeric network through a green protocol to obtain transparent hydrogels (ALP@AETA) that can be stored at room temperature and potentially used as a disposable biosensor platform for the rapid detection of ALP inhibitors. For this purpose, different strategies for the immobilization of ALP in the hydrogel were examined and the properties of the new material, compared to the hydrogel in the absence of enzyme, were studied. The conformation and stability of the immobilized enzyme were characterized by monitoring the changes in its intrinsic fluorescence as a function of temperature, in order to study the unfolding/folding process inside the hydrogel, inherently related to the enzyme activity. The results show that the immobilized enzyme retains its activity, slightly increases its thermal stability and can be stored as a xerogel at room temperature without losing its properties. A small portion of a few millimeters of ALP@AETA xerogel was sufficient to perform enzymatic activity inhibition assays, so as a proof of concept, the device was tested as a portable optical biosensor for the detection of phosphate in water with satisfactory results. Given the good stability of the ALP@AETA xerogel and the interesting applications of ALP, not only in the environmental field but also as a therapeutic enzyme, we believe that this study could be of great use for the development of new devices for sensing and protein delivery. MDPI 2023-01-31 /pmc/articles/PMC9917215/ /pubmed/36769007 http://dx.doi.org/10.3390/ijms24032672 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alacid, Yolanda
Martínez-Tomé, María José
Esquembre, Rocío
Herrero, M. Antonia
Mateo, C. Reyes
Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing
title Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing
title_full Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing
title_fullStr Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing
title_full_unstemmed Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing
title_short Portable Alkaline Phosphatase–Hydrogel Platform: From Enzyme Characterization to Phosphate Sensing
title_sort portable alkaline phosphatase–hydrogel platform: from enzyme characterization to phosphate sensing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917215/
https://www.ncbi.nlm.nih.gov/pubmed/36769007
http://dx.doi.org/10.3390/ijms24032672
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