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Confinement of Triple-Enzyme-Involved Antioxidant Cascade in Two-Dimensional Nanostructure
[Image: see text] Application of antioxidant enzymes in medical or industrial processes is limited due to their high sensitivity to environmental conditions. Incorporation of such enzymes in nanostructures provides a promising route to obtain highly efficient and robust biocatalytic system to scaven...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9906813/ https://www.ncbi.nlm.nih.gov/pubmed/36776691 http://dx.doi.org/10.1021/acsmaterialslett.2c00580 |
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author | Szerlauth, Adel Varga, Árpád Madácsy, Tamara Sebők, Dániel Bashiri, Sahra Skwarczynski, Mariusz Toth, Istvan Maléth, József Szilagyi, Istvan |
author_facet | Szerlauth, Adel Varga, Árpád Madácsy, Tamara Sebők, Dániel Bashiri, Sahra Skwarczynski, Mariusz Toth, Istvan Maléth, József Szilagyi, Istvan |
author_sort | Szerlauth, Adel |
collection | PubMed |
description | [Image: see text] Application of antioxidant enzymes in medical or industrial processes is limited due to their high sensitivity to environmental conditions. Incorporation of such enzymes in nanostructures provides a promising route to obtain highly efficient and robust biocatalytic system to scavenge reactive oxygen species (ROS). Here, this question was addressed by confinement of superoxide dismutase (SOD), horseradish peroxidase (HRP), and catalase (CAT) enzymes into nanostructures containing polyelectrolyte building blocks (alginate (Alg) and trimethyl chitosan (TMC)) and delaminated layered double hydroxide (dLDH) nanoparticle support. The nanocomposite possessed excellent structural and colloidal stability, while antioxidant tests revealed that the enzymes remained active upon immobilization and the developed composite greatly reduced intracellular oxidative stress in two-dimensional cell cultures. Moreover, it effectively prevented hydrogen peroxide-induced double stranded DNA breaks, which is a common consequence of oxidative stress. The results provide important tools to design complex nanostructures with multienzymatic antioxidant activities for ROS scavenging. |
format | Online Article Text |
id | pubmed-9906813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99068132023-02-08 Confinement of Triple-Enzyme-Involved Antioxidant Cascade in Two-Dimensional Nanostructure Szerlauth, Adel Varga, Árpád Madácsy, Tamara Sebők, Dániel Bashiri, Sahra Skwarczynski, Mariusz Toth, Istvan Maléth, József Szilagyi, Istvan ACS Mater Lett [Image: see text] Application of antioxidant enzymes in medical or industrial processes is limited due to their high sensitivity to environmental conditions. Incorporation of such enzymes in nanostructures provides a promising route to obtain highly efficient and robust biocatalytic system to scavenge reactive oxygen species (ROS). Here, this question was addressed by confinement of superoxide dismutase (SOD), horseradish peroxidase (HRP), and catalase (CAT) enzymes into nanostructures containing polyelectrolyte building blocks (alginate (Alg) and trimethyl chitosan (TMC)) and delaminated layered double hydroxide (dLDH) nanoparticle support. The nanocomposite possessed excellent structural and colloidal stability, while antioxidant tests revealed that the enzymes remained active upon immobilization and the developed composite greatly reduced intracellular oxidative stress in two-dimensional cell cultures. Moreover, it effectively prevented hydrogen peroxide-induced double stranded DNA breaks, which is a common consequence of oxidative stress. The results provide important tools to design complex nanostructures with multienzymatic antioxidant activities for ROS scavenging. American Chemical Society 2023-01-18 /pmc/articles/PMC9906813/ /pubmed/36776691 http://dx.doi.org/10.1021/acsmaterialslett.2c00580 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Szerlauth, Adel Varga, Árpád Madácsy, Tamara Sebők, Dániel Bashiri, Sahra Skwarczynski, Mariusz Toth, Istvan Maléth, József Szilagyi, Istvan Confinement of Triple-Enzyme-Involved Antioxidant Cascade in Two-Dimensional Nanostructure |
title | Confinement
of Triple-Enzyme-Involved Antioxidant
Cascade in Two-Dimensional Nanostructure |
title_full | Confinement
of Triple-Enzyme-Involved Antioxidant
Cascade in Two-Dimensional Nanostructure |
title_fullStr | Confinement
of Triple-Enzyme-Involved Antioxidant
Cascade in Two-Dimensional Nanostructure |
title_full_unstemmed | Confinement
of Triple-Enzyme-Involved Antioxidant
Cascade in Two-Dimensional Nanostructure |
title_short | Confinement
of Triple-Enzyme-Involved Antioxidant
Cascade in Two-Dimensional Nanostructure |
title_sort | confinement
of triple-enzyme-involved antioxidant
cascade in two-dimensional nanostructure |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9906813/ https://www.ncbi.nlm.nih.gov/pubmed/36776691 http://dx.doi.org/10.1021/acsmaterialslett.2c00580 |
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