κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme Immobilization

During the last few decades, polysaccharide hydrogels attract more and more attention as therapeutic protein delivery systems due to their biocompatibility and the simplicity of the biodegradation of natural polymers. The protein retention by and release from the polysaccharide gel network is regula...

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Main Authors: Olga N. Makshakova, Liliya R. Bogdanova, Anastasiya O. Makarova, Aleksandra M. Kusova, Elena A. Ermakova, Mariia A. Kazantseva, Yuriy F. Zuev
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/14/19/4071
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author Olga N. Makshakova
Liliya R. Bogdanova
Anastasiya O. Makarova
Aleksandra M. Kusova
Elena A. Ermakova
Mariia A. Kazantseva
Yuriy F. Zuev
author_facet Olga N. Makshakova
Liliya R. Bogdanova
Anastasiya O. Makarova
Aleksandra M. Kusova
Elena A. Ermakova
Mariia A. Kazantseva
Yuriy F. Zuev
author_sort Olga N. Makshakova
collection DOAJ
description During the last few decades, polysaccharide hydrogels attract more and more attention as therapeutic protein delivery systems due to their biocompatibility and the simplicity of the biodegradation of natural polymers. The protein retention by and release from the polysaccharide gel network is regulated by geometry and physical interactions of protein with the matrix. In the present work, we studied the molecular details of interactions between κ-carrageenan and three lipases, namely the lipases from <i>Candida rugosa</i>, <i>Mucor javanicus</i>, and <i>Rhizomucor miehei</i>—which differ in their size and net charge—upon protein immobilization in microparticles of polysaccharide gel. The kinetics of protein release revealed the different capability of κ-carrageenan to retain lipases, which are generally negatively charged; that was shown to be in line with the energy of interactions between polysaccharides and positively charged epitopes on the protein surface. These data create a platform for the novel design of nanocarriers for biomedical probes of enzymatic origin.
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spelling doaj.art-1fe055ae58a64518a412b7885bf157a92023-11-23T21:33:45ZengMDPI AGPolymers2073-43602022-09-011419407110.3390/polym14194071κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme ImmobilizationOlga N. Makshakova0Liliya R. Bogdanova1Anastasiya O. Makarova2Aleksandra M. Kusova3Elena A. Ermakova4Mariia A. Kazantseva5Yuriy F. Zuev6Kazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky St., 2/31, 420111 Kazan, RussiaKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky St., 2/31, 420111 Kazan, RussiaKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky St., 2/31, 420111 Kazan, RussiaKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky St., 2/31, 420111 Kazan, RussiaKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky St., 2/31, 420111 Kazan, RussiaKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky St., 2/31, 420111 Kazan, RussiaKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky St., 2/31, 420111 Kazan, RussiaDuring the last few decades, polysaccharide hydrogels attract more and more attention as therapeutic protein delivery systems due to their biocompatibility and the simplicity of the biodegradation of natural polymers. The protein retention by and release from the polysaccharide gel network is regulated by geometry and physical interactions of protein with the matrix. In the present work, we studied the molecular details of interactions between κ-carrageenan and three lipases, namely the lipases from <i>Candida rugosa</i>, <i>Mucor javanicus</i>, and <i>Rhizomucor miehei</i>—which differ in their size and net charge—upon protein immobilization in microparticles of polysaccharide gel. The kinetics of protein release revealed the different capability of κ-carrageenan to retain lipases, which are generally negatively charged; that was shown to be in line with the energy of interactions between polysaccharides and positively charged epitopes on the protein surface. These data create a platform for the novel design of nanocarriers for biomedical probes of enzymatic origin.https://www.mdpi.com/2073-4360/14/19/4071polysaccharidesnanogelsenzymesimmobilizationdelivery systems
spellingShingle Olga N. Makshakova
Liliya R. Bogdanova
Anastasiya O. Makarova
Aleksandra M. Kusova
Elena A. Ermakova
Mariia A. Kazantseva
Yuriy F. Zuev
κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme Immobilization
Polymers
polysaccharides
nanogels
enzymes
immobilization
delivery systems
title κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme Immobilization
title_full κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme Immobilization
title_fullStr κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme Immobilization
title_full_unstemmed κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme Immobilization
title_short κ-Carrageenan Hydrogel as a Matrix for Therapeutic Enzyme Immobilization
title_sort κ carrageenan hydrogel as a matrix for therapeutic enzyme immobilization
topic polysaccharides
nanogels
enzymes
immobilization
delivery systems
url https://www.mdpi.com/2073-4360/14/19/4071
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