Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1784886316993871872 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9917215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT alacidyolanda portablealkalinephosphatasehydrogelplatformfromenzymecharacterizationtophosphatesensing AT martineztomemariajose portablealkalinephosphatasehydrogelplatformfromenzymecharacterizationtophosphatesensing AT esquembrerocio portablealkalinephosphatasehydrogelplatformfromenzymecharacterizationtophosphatesensing AT herreromantonia portablealkalinephosphatasehydrogelplatformfromenzymecharacterizationtophosphatesensing AT mateocreyes portablealkalinephosphatasehydrogelplatformfromenzymecharacterizationtophosphatesensing |