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Immobilization of fibrinolytic protease from Mucor subtilissimus UCP 1262 in magnetic nanoparticles.
Marques da Silva, Marllyn; Wanderley Duarte Neto, José Manoel; Barros Regueira, Bruno Vinícius; Torres do Couto, Milena Tereza; Vitória da Silva Sobral, Renata; Sales Conniff, Amanda Emmanuelle; Pedrosa Brandão Costa, Romero Marcos; Cajubá de Britto Lira Nogueira, Mariane; Pereira da Silva Santos, Noemia; Pastrana, Lorenzo; Lima Leite, Ana Cristina; Converti, Attilio; Nascimento, Thiago Pajeú; Figueiredo Porto, Ana Lúcia.
Afiliação
  • Marques da Silva M; Laboratory of Nanotechnology, Biotechnology and Cell Culture, Academic Center of Vitória, Federal University of Pernambuco, 55608-680, Vitória de Santo Antão, Pernambuco, Brazil.
  • Wanderley Duarte Neto JM; Laboratory of Bioactive Technology, Department of Morphology and Animal Physiology, Federal Rural University of Pernambuco, Rua Dom Manoel de Medeiros, s/n, Dois Irmãos, 52171-900, Recife, Pernambuco, Brazil.
  • Barros Regueira BV; Laboratory of Research in Biotechnology and Hemoderivatives, Department of Pharmaceutical Sciences, Federal University of Pernambuco, 50670-420, Recife, Pernambuco, Brazil.
  • Torres do Couto MT; Laboratory of Research in Biotechnology and Hemoderivatives, Department of Pharmaceutical Sciences, Federal University of Pernambuco, 50670-420, Recife, Pernambuco, Brazil.
  • Vitória da Silva Sobral R; Laboratory of Research in Biotechnology and Hemoderivatives, Department of Pharmaceutical Sciences, Federal University of Pernambuco, 50670-420, Recife, Pernambuco, Brazil.
  • Sales Conniff AE; Department of Molecular Medicine- College of Medicine, University of South Florida, Bruce B. Downs Blvd, MDC 3518, 12901, Tampa, FL, United States.
  • Pedrosa Brandão Costa RM; Laboratory of Advances in Protein Biotechnology (LABIOPROT), Institute of Biological Sciences, University of Pernambuco, Rua Arnóbio Marquês, 310 - Santo Amaro, Recife - PE, 50100-130, Recife, Pernambuco, Brazil.
  • Cajubá de Britto Lira Nogueira M; Laboratory of Nanotechnology, Biotechnology and Cell Culture, Academic Center of Vitória, Federal University of Pernambuco, 55608-680, Vitória de Santo Antão, Pernambuco, Brazil.
  • Pereira da Silva Santos N; Laboratory of Nanotechnology, Biotechnology and Cell Culture, Academic Center of Vitória, Federal University of Pernambuco, 55608-680, Vitória de Santo Antão, Pernambuco, Brazil.
  • Pastrana L; International Iberian Nanotechnology Laboratory, Av. Mestre José Veiga, Braga, 4715-330, Portugal.
  • Lima Leite AC; Laboratory of Research in Biotechnology and Hemoderivatives, Department of Pharmaceutical Sciences, Federal University of Pernambuco, 50670-420, Recife, Pernambuco, Brazil.
  • Converti A; Department of Civil, Chemical and Environmental Engineering, Pole of Chemical Engineering, University of Genoa, Via Opera Pia 15, I-16145 Genoa, Italy.
  • Nascimento TP; Laboratory of Bioactive Technology, Department of Morphology and Animal Physiology, Federal Rural University of Pernambuco, Rua Dom Manoel de Medeiros, s/n, Dois Irmãos, 52171-900, Recife, Pernambuco, Brazil.
  • Figueiredo Porto AL; Laboratory of Bioactive Technology, Department of Morphology and Animal Physiology, Federal Rural University of Pernambuco, Rua Dom Manoel de Medeiros, s/n, Dois Irmãos, 52171-900, Recife, Pernambuco, Brazil. Electronic address: analuporto@yahoo.com.br.
Protein Expr Purif ; 192: 106044, 2022 04.
Article em En | MEDLINE | ID: mdl-34998976
ABSTRACT
This work reports the immobilization of a fibrinolytic protease (FP) from Mucor subtilissimus UCP 1262 on Fe3O4 magnetic nanoparticles (MNPs) produced by precipitation of FeCl3·6H2O and FeCl2·4H2O, 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeo Hidrolases / Nanopartículas de Magnetita / Fibrinolíticos / Mucor Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeo Hidrolases / Nanopartículas de Magnetita / Fibrinolíticos / Mucor Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article