Nitrilotriacetic Acid Functionalized Microgels for Efficient Immobilization of Hyaluronan Synthase.

biomaterials enzyme immobilization metal affinity binding microgels polysaccharides

Journal

Macromolecular bioscience
ISSN: 1616-5195
Titre abrégé: Macromol Biosci
Pays: Germany
ID NLM: 101135941

Informations de publication

Date de publication:
17 Jul 2024
Historique:
revised: 23 05 2024
received: 20 02 2024
medline: 17 7 2024
pubmed: 17 7 2024
entrez: 17 7 2024
Statut: aheadofprint

Résumé

Enzymes play a vital role in synthesizing complex biological molecules like hyaluronic acid (HA). Immobilizing enzymes on support materials is essential for their efficient use and reuse in multiple cycles. Microgels, composed of cross-linked, highly swollen polymer networks, are ideal for enzyme uptake owing to their high porosity. This study demonstrates the immobilization of His

Identifiants

pubmed: 39018489
doi: 10.1002/mabi.202400075
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2400075

Subventions

Organisme : European Commission
ID : 300088302
Organisme : Bundesministerium für Bildung und Forschung
ID : 031B1116A
Organisme : Bundesministerium für Bildung und Forschung
ID : 031B1116B

Informations de copyright

© 2024 The Author(s). Macromolecular Bioscience published by Wiley‐VCH GmbH.

Références

Hansen, I. M., Ebbesen, M. F., Kaspersen, L., Thomsen, T., Bienk, K., Cai, Y., Malle, B. M., Howard, K. A., Mol. Pharmaceutics 2017, 14, 2359.
N. M. Salwowska, K. A. Bebenek, D. A. Żądło, D. L. Wcisło‐Dziadecka, J Cosmet Dermatol 2016, 15, 520.
A. M. Juncan, D. G. Moisă, A. Santini, C. Morgovan, L. L. Rus, A. L. Vonica‐Țincu, F. Loghin, Molecules 2021, 26, 4429.
M. Qiao, J. Zhang, J. Li, L. Xing, X. Zhou, Y. Xie, X. Zhang, Process Biochem 2023, 133, 261.
Y. Qiu, Y. Ma, Y. Huang, S. Li, H. Xu, E. Su, Carbohydr. Polym. 2021, 269, 118320.
J. Gottschalk, M. Aßmann, J. Kuballa, L. Elling, ChemSusChem 2022, 15, 202101071.
J. Gottschalk, L. Elling, Curr. Opin. Chem. Biol. 2021, 61, 71.
J. H. Sze, J. C. Brownlie, C. A. Love, Biotech 2016, 6, 67.
P. L. DeAngelis, Cell. Mol. Life Sci. 1999, 56, 670.
P. L. DeAngelis, J. Zimmer, Glycobiology 2023, 33, 1117.
M. Nöth, E. Gau, F. Jung, M. D. Davari, I. El‐Awaad, A. Pich, U. Schwaneberg, Green Chem. 2020, 22, 8183.
A. A. Homaei, R. Sariri, F. Vianello, R. Stevanato, J Chem Biol 2013, 6, 185.
P. Torres‐Salas, A. Del Monte‐Martinez, B. Cutiño‐Avila, B. Rodriguez‐Colinas, M. Alcalde, A. O. Ballesteros, F. J. Plou, Adv. Mater. 2011, 23, 5275.
R. A. Sheldon, Adv. Synth. Catal. 2007, 349, 1289.
M. N. Gupta, M. Kaloti, M. Kapoor, K. Solanki, Art. Cells, Blood Subs., and Immob. 2011, 39, 98.
R. A. Sheldon, A. Basso, D. Brady, Chem. Soc. Rev. 2021, 50, 5850.
L. Cao, Curr. Opin. Chem. Biol. 2005, 9, 217.
M. Karg, A. Pich, T. Hellweg, T. Hoare, L. A. Lyon, J. J. Crassous, D. Suzuki, R. A. Gumerov, S. Schneider, I. I. Potemkin, W. Richtering, Langmuir 2019, 35, 6231.
F. A. Plamper, W. Richtering, Acc. Chem. Res. 2017, 50, 131.
J. Oberdisse, T. Hellweg, Colloid Polym. Sci. 2020, 298, 921.
J. M. Guisan, Ed. Methods in Biotechnology, Humana Press, Totowa, NJ 2006, 22.
J. M. Guisan, Ed. Methods in Biotechnology, 2006, Humana Press, USA 2006, 22.
B. Mizrahi, S. Irusta, M. McKenna, C. Stefanescu, L. Yedidsion, M. Myint, R. Langer, D. S. Kohane, Adv. Mater. 2011, 23, H258.
J. Porath, B. Olin, Biochem 1983, 1621.
V. Gaberc‐Porekar, V. Menart, J. Biochem. Biophys. Methods 2001, 49, 335.
H. Block, B. Maertens, A. Spriestersbach, N. Brinker, J. Kubicek, R. Fabis, J. Labahn, F. Schäfer, Methods Enzymol 2009, 463, 439.
T. Heida, T. Köhler, A. Kaufmann, M. J. Männel, J. Thiele, Chem Syst. Chem. 2020, 2, e1900058.
T. Köhler, T. Heida, S. Hoefgen, N. Weigel, V. Valiante, J. Thiele, RSC Adv. 2020, 10, 40588.
H. Xu, B. Wei, X. Liu, Y. Huang, W. Zhou, H. Liang, Biochem. Eng. J. 2022, 180, 108362.
I. K. Sommerfeld, H. Malyaran, S. Neuss, D. E. Demco, A. Pich, Biomacromolecules 2024, 25, 903.
P. L. DeAngelis, L. C. Oatman, D. F. Gay, J. Biol. Chem. 2003, 278, 35199.
T. Mori, A. Hirose, T. Hagiwara, M. Ohtsuka, Y. Kakuta, K. Kimata, Y. Okahata, J. Am. Chem. Soc. 2012, 134, 20254.
L. C. Kröger, W. A. Kopp, K. Leonhard, J. Phys. Chem. B 2017, 121, 2887.
F. Grabowski, V. S. Petrovskii, F. Fink, D. E. Demco, S. Herres‐Pawlis, I. I. Potemkin, A. Pich, Adv. Sci. 2022, 9, e2204853.
H. M. Irving, M. G. Miles, L. D. Pettit, Anal. Chim. Acta 1967, 38, 475.
A. K. Das, Transition Met. Chem. 1990, 15, 75.
Y. Tomita, K. Ueno, Bull. Chem. Soc. Jpn. 1963, 36, 1069.
R. L. Anderson, W. E. Bishop, R. L. Campbell, Crit. Rev. Toxicol. 1985, 15, 1.
A. E. Martell, R. M. Smith, Critical Stability Constants: Inorganic Complexes, Springer, New York, NY 1976.
A. Mourran, Y. Wu, R. A. Gumerov, A. A. Rudov, I. I. Potemkin, Langmuir 2016, 32, 723.
L. Hoppe Alvarez, A. A. Rudov, R. A. Gumerov, P. Lenssen, U. Simon, I. I. Potemkin, D. Wöll, Phys. Chem. Chem. Phys. 2021, 23, 4927.
M. A. Salam, K. Aoki, Inorg. Chim. Acta 2000, 311, 15.
N. H. Dung, B. Viossat, A. Busnot, J. M. González Pérez, S. González García, Inorg. Chem. 1988, 27, 1227.
E. Souaya, W. Hanna, E. Ismail, N. Milad, Molecules 2000, 5, 1121.
M. S. Zetter, M. W. Grant, E. J. Wood, H. W. Dodgen, J. P. Hunt, Inorg. Chem. 1972, 11, 2701.
R. J. Motekaitis, A. E. Martell, J. Coord. Chem. 1994, 31, 67.
M. A. Walters, V. Vapnyar, A. Bolour, C. Incarvito, A. L. Rheingold, Polyhedron 2003, 22, 941.
K. Sawada, W. Duan, M. Ono, K. Satoh, J Chem Soc 2000, Dalton Trans. 919.
G. Chaga, D. E. Bochkariov, G. G. Jokhadze, J. Hopp, P. Nelson, J. Chromatogr. A 1999, 864, 247.
J. Gottschalk, H. Zaun, A. Eisele, J. Kuballa, L. Elling, Int. J. Mol. Sci. 2019, 20, 5664.
A. Eisele, H. Zaun, J. Kuballa, L. Elling, ChemCatChem 2018, 10, 2969.
L. Büdinger, M. Hertl, Allergy 2000, 55, 108.
M. Horie, K. Nishio, K. Fujita, H. Kato, A. Nakamura, S. Kinugasa, S. Endoh, A. Miyauchi, K. Yamamoto, H. Murayama, E. Niki, H. Iwahashi, Y. Yoshida, J. Nakanishi, Chem. Res. Toxicol. 2009, 22, 1415.
W. Jia, M. W. Beatty, R. A. Reinhardt, T. M. Petro, D. M. Cohen, C. R. Maze, E. A. Strom, M. Hoffman, J Biomed Mater Res 1999, 48, 488.
W. Jing, P. L. DeAngelis, J. Biol. Chem. 2004, 279, 42345.
N. C. Pan, H. C. B. Pereira, M. d. L. C. Da Silva, F. D. A. Vasconcelos, M. A. P. C Celligoi, Appl. Biochem. Biotechnol. 2017, 182, 276.
R. Gilli, M. Kacuráková, M. Mathlouthi, L. Navarini, S. Paoletti, Carbohydr. Res. 1994, 263, 315.

Auteurs

Isabel Katja Sommerfeld (IK)

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074, Aachen, Germany.
DWI - Leibniz-Institute for Interactive Materials e.V., Forckenbeckstraße 50, 52074, Aachen, Germany.

Esther Maria Dälken (EM)

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074, Aachen, Germany.
DWI - Leibniz-Institute for Interactive Materials e.V., Forckenbeckstraße 50, 52074, Aachen, Germany.

Lothar Elling (L)

Laboratory for Biomaterials, Institute of Biotechnology and Helmholtz-Institute for Biomedical Engineering, RWTH Aachen University, Pauwelsstraße 20, 52074, Aachen, Germany.

Andrij Pich (A)

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074, Aachen, Germany.
DWI - Leibniz-Institute for Interactive Materials e.V., Forckenbeckstraße 50, 52074, Aachen, Germany.
Aachen Maastricht Institute for Biobased Materials (AMIBM), Maastricht University, Brightlands Chemelot Campus, Urmonderbaan 22, RD Geleen, 6167, The Netherlands.

Classifications MeSH