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Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system()
OBJECTIVE: CYP1A2 and NADPH-CYP450 oxidoreductase (POR) were expressed in the baculovirus/Spodoptera frugiperda (sf9) system. The aim of this study was to investigate the effects of heme precursors on the expression of CYP1A2 and POR. METHODS: The heme precursors [δ-Aminolaevulinic Acid (5-ALA), Fe(...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial Department of Journal of Biomedical Research
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596560/ https://www.ncbi.nlm.nih.gov/pubmed/23554636 http://dx.doi.org/10.1016/S1674-8301(10)60034-6 |
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author | Lu, Huiyuan Ma, Jun Liu, Nian Wang, Shoulin |
author_facet | Lu, Huiyuan Ma, Jun Liu, Nian Wang, Shoulin |
author_sort | Lu, Huiyuan |
collection | PubMed |
description | OBJECTIVE: CYP1A2 and NADPH-CYP450 oxidoreductase (POR) were expressed in the baculovirus/Spodoptera frugiperda (sf9) system. The aim of this study was to investigate the effects of heme precursors on the expression of CYP1A2 and POR. METHODS: The heme precursors [δ-Aminolaevulinic Acid (5-ALA), Fe(3+) and hemin] were introduced into the system to evaluate their effects on the expression of CYP1A2, POR and their co-expression. All the proteins were identified using immunoblotting, CO-difference spectroscopy, or cytochrome c assay. RESULTS: In the present study, functional CYP1A2 and POR were successfully expressed in the baculovirus/sf9 system, and both of them showed high activities. Co-addition of 5-ALA and Fe(3+) significantly improved expression of CYP1A2 by about 50% compared with the addition of 5-ALA, Fe(3+) or hemin alone. Either co-addition of 5-ALA and Fe(3+) or addition of 5-ALA or Fe(3+) alone improved the POR expression level 2 fold and its activity 7-10 fold compared with control (no addition). However, unlike CYP1A2, there was no difference between the co-addition and addition of these heme precursors alone. Different ratios of BvCYP1A2 to BvPOR also affected the co-expression of CYP1A2 and POR, with a 3:1 ratio of BvCYP1A2 / BvPOR significantly increasing their co-expression. Surprisingly, the addition of 0.1 mM 5-ALA or Fe(3+) alone, but not their co-addition, could significantly improve the CYP1A2 and POR co-expression (P < 0.05). CONCLUSION: 5-ALA and Fe(3+) increased the expression of CYP1A2 and POR in a baculovirus/sf9 system, but the pattern of their expression was different between their expression alone and co-expression. |
format | Online Article Text |
id | pubmed-3596560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Editorial Department of Journal of Biomedical Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-35965602013-04-02 Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system() Lu, Huiyuan Ma, Jun Liu, Nian Wang, Shoulin J Biomed Res Research Paper OBJECTIVE: CYP1A2 and NADPH-CYP450 oxidoreductase (POR) were expressed in the baculovirus/Spodoptera frugiperda (sf9) system. The aim of this study was to investigate the effects of heme precursors on the expression of CYP1A2 and POR. METHODS: The heme precursors [δ-Aminolaevulinic Acid (5-ALA), Fe(3+) and hemin] were introduced into the system to evaluate their effects on the expression of CYP1A2, POR and their co-expression. All the proteins were identified using immunoblotting, CO-difference spectroscopy, or cytochrome c assay. RESULTS: In the present study, functional CYP1A2 and POR were successfully expressed in the baculovirus/sf9 system, and both of them showed high activities. Co-addition of 5-ALA and Fe(3+) significantly improved expression of CYP1A2 by about 50% compared with the addition of 5-ALA, Fe(3+) or hemin alone. Either co-addition of 5-ALA and Fe(3+) or addition of 5-ALA or Fe(3+) alone improved the POR expression level 2 fold and its activity 7-10 fold compared with control (no addition). However, unlike CYP1A2, there was no difference between the co-addition and addition of these heme precursors alone. Different ratios of BvCYP1A2 to BvPOR also affected the co-expression of CYP1A2 and POR, with a 3:1 ratio of BvCYP1A2 / BvPOR significantly increasing their co-expression. Surprisingly, the addition of 0.1 mM 5-ALA or Fe(3+) alone, but not their co-addition, could significantly improve the CYP1A2 and POR co-expression (P < 0.05). CONCLUSION: 5-ALA and Fe(3+) increased the expression of CYP1A2 and POR in a baculovirus/sf9 system, but the pattern of their expression was different between their expression alone and co-expression. Editorial Department of Journal of Biomedical Research 2010-05 /pmc/articles/PMC3596560/ /pubmed/23554636 http://dx.doi.org/10.1016/S1674-8301(10)60034-6 Text en © 2010 by the Journal of Biomedical Research. All rights reserved. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Research Paper Lu, Huiyuan Ma, Jun Liu, Nian Wang, Shoulin Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system() |
title | Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system() |
title_full | Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system() |
title_fullStr | Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system() |
title_full_unstemmed | Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system() |
title_short | Effects of heme precursors on CYP1A2 and POR expression in the baculovirus/Spodoptera frugiperda system() |
title_sort | effects of heme precursors on cyp1a2 and por expression in the baculovirus/spodoptera frugiperda system() |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596560/ https://www.ncbi.nlm.nih.gov/pubmed/23554636 http://dx.doi.org/10.1016/S1674-8301(10)60034-6 |
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