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Immobilization of fibrinolytic protease from Mucor subtilissimus UCP 1262 in magnetic nanoparticles.

Authors :
Marques da Silva M
Wanderley Duarte Neto JM
Barros Regueira BV
Torres do Couto MT
Vitória da Silva Sobral R
Sales Conniff AE
Pedrosa Brandão Costa RM
Cajubá de Britto Lira Nogueira M
Pereira da Silva Santos N
Pastrana L
Lima Leite AC
Converti A
Nascimento TP
Figueiredo Porto AL
Source :
Protein expression and purification [Protein Expr Purif] 2022 Apr; Vol. 192, pp. 106044. Date of Electronic Publication: 2022 Jan 06.
Publication Year :
2022

Abstract

This work reports the immobilization of a fibrinolytic protease (FP) from Mucor subtilissimus UCP 1262 on Fe <subscript>3</subscript> O <subscript>4</subscript> magnetic nanoparticles (MNPs) produced by precipitation of FeCl <subscript>3</subscript> ·6H <subscript>2</subscript> O and FeCl <subscript>2</subscript> ·4H <subscript>2</subscript> O, coated with polyaniline and activated with glutaraldehyde. The FP was obtained by solid state fermentation, precipitated with 40-60% ammonium sulfate, and purified by DEAE-Sephadex A50 ion exchange chromatography. The FP immobilization procedure allowed for an enzyme retention of 52.13%. The fibrinolytic protease immobilized on magnetic nanoparticles (MNPs/FP) maintained more than 60% of activity at a temperature of 40 to 60 °C and at pH 7 to 10, when compared to the non-immobilized enzyme. MNPs and MNPs/FP did not show any cytotoxicity against HEK-293 and J774A.1 cells. MNPs/FP was not hemolytic and reduced the hemolysis induced by MNPs from 2.07% to 1.37%. Thrombus degradation by MNPs/FP demonstrated that the immobilization process guaranteed the thrombolytic activity of the enzyme. MNPs/FP showed a total degradation of the γ chain of human fibrinogen within 90 min. These results suggest that MNPs/FP may be used as an alternative strategy to treat cardiovascular diseases with a targeted release through an external magnetic field.<br /> (Copyright © 2022 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1096-0279
Volume :
192
Database :
MEDLINE
Journal :
Protein expression and purification
Publication Type :
Academic Journal
Accession number :
34998976
Full Text :
https://doi.org/10.1016/j.pep.2022.106044