Cargando…

Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)

A prospective technology for reversible enzyme complexation accompanied with its inactivation and protection followed by reactivation after a fast thermocontrolled release has been demonstrated. A thermoresponsive polymer with upper critical solution temperature, poly(N-acryloyl glycinamide) (PNAGA)...

Descripción completa

Detalles Bibliográficos
Autores principales: Semenyuk, Pavel I., Kurochkina, Lidia P., Mäkinen, Lauri, Muronetz, Vladimir I., Hietala, Sami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540930/
https://www.ncbi.nlm.nih.gov/pubmed/34685360
http://dx.doi.org/10.3390/polym13203601
_version_ 1784589106094800896
author Semenyuk, Pavel I.
Kurochkina, Lidia P.
Mäkinen, Lauri
Muronetz, Vladimir I.
Hietala, Sami
author_facet Semenyuk, Pavel I.
Kurochkina, Lidia P.
Mäkinen, Lauri
Muronetz, Vladimir I.
Hietala, Sami
author_sort Semenyuk, Pavel I.
collection PubMed
description A prospective technology for reversible enzyme complexation accompanied with its inactivation and protection followed by reactivation after a fast thermocontrolled release has been demonstrated. A thermoresponsive polymer with upper critical solution temperature, poly(N-acryloyl glycinamide) (PNAGA), which is soluble in water at elevated temperatures but phase separates at low temperatures, has been shown to bind lysozyme, chosen as a model enzyme, at a low temperature (10 °C and lower) but not at room temperature (around 25 °C). The cooling of the mixture of PNAGA and lysozyme solutions from room temperature resulted in the capturing of the protein and the formation of stable complexes; heating it back up was accompanied by dissolving the complexes and the release of the bound lysozyme. Captured by the polymer, lysozyme was inactive, but a temperature-mediated release from the complexes was accompanied by its reactivation. Complexation also partially protected lysozyme from proteolytic degradation by proteinase K, which is useful for biotechnological applications. The obtained results are relevant for important medicinal tasks associated with drug delivery such as the delivery and controlled release of enzyme-based drugs.
format Online
Article
Text
id pubmed-8540930
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-85409302021-10-24 Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide) Semenyuk, Pavel I. Kurochkina, Lidia P. Mäkinen, Lauri Muronetz, Vladimir I. Hietala, Sami Polymers (Basel) Article A prospective technology for reversible enzyme complexation accompanied with its inactivation and protection followed by reactivation after a fast thermocontrolled release has been demonstrated. A thermoresponsive polymer with upper critical solution temperature, poly(N-acryloyl glycinamide) (PNAGA), which is soluble in water at elevated temperatures but phase separates at low temperatures, has been shown to bind lysozyme, chosen as a model enzyme, at a low temperature (10 °C and lower) but not at room temperature (around 25 °C). The cooling of the mixture of PNAGA and lysozyme solutions from room temperature resulted in the capturing of the protein and the formation of stable complexes; heating it back up was accompanied by dissolving the complexes and the release of the bound lysozyme. Captured by the polymer, lysozyme was inactive, but a temperature-mediated release from the complexes was accompanied by its reactivation. Complexation also partially protected lysozyme from proteolytic degradation by proteinase K, which is useful for biotechnological applications. The obtained results are relevant for important medicinal tasks associated with drug delivery such as the delivery and controlled release of enzyme-based drugs. MDPI 2021-10-19 /pmc/articles/PMC8540930/ /pubmed/34685360 http://dx.doi.org/10.3390/polym13203601 Text en © 2021 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
Semenyuk, Pavel I.
Kurochkina, Lidia P.
Mäkinen, Lauri
Muronetz, Vladimir I.
Hietala, Sami
Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)
title Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)
title_full Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)
title_fullStr Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)
title_full_unstemmed Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)
title_short Thermocontrolled Reversible Enzyme Complexation-Inactivation-Protection by Poly(N-acryloyl glycinamide)
title_sort thermocontrolled reversible enzyme complexation-inactivation-protection by poly(n-acryloyl glycinamide)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540930/
https://www.ncbi.nlm.nih.gov/pubmed/34685360
http://dx.doi.org/10.3390/polym13203601
work_keys_str_mv AT semenyukpaveli thermocontrolledreversibleenzymecomplexationinactivationprotectionbypolynacryloylglycinamide
AT kurochkinalidiap thermocontrolledreversibleenzymecomplexationinactivationprotectionbypolynacryloylglycinamide
AT makinenlauri thermocontrolledreversibleenzymecomplexationinactivationprotectionbypolynacryloylglycinamide
AT muronetzvladimiri thermocontrolledreversibleenzymecomplexationinactivationprotectionbypolynacryloylglycinamide
AT hietalasami thermocontrolledreversibleenzymecomplexationinactivationprotectionbypolynacryloylglycinamide