Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3)
Background: Recombinant human interleukin-1 receptor antagonist (IL-1RA) is a protein with 153 amino acids and molecular weight of 16.83 kDa. This drug protein is known as Anakinra, and has an effective application in the treatment of rheumatoid arthritis. This study was conducted to examine the pro...
| Published in: | مجله دانشکده پزشکی اصفهان |
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| Main Authors: | , , |
| Format: | Article |
| Language: | Persian |
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Isfahan University of Medical Sciences
2019-11-01
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| Subjects: | |
| Online Access: | http://jims.mui.ac.ir/index.php/jims/article/view/12229 |
| _version_ | 1851831619754655744 |
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| author | Hanieh Fardgoli Seyed Nezameddin Hoseini Setareh Haghighat |
| author_facet | Hanieh Fardgoli Seyed Nezameddin Hoseini Setareh Haghighat |
| author_sort | Hanieh Fardgoli |
| collection | DOAJ |
| container_title | مجله دانشکده پزشکی اصفهان |
| description | Background: Recombinant human interleukin-1 receptor antagonist (IL-1RA) is a protein with 153 amino acids and molecular weight of 16.83 kDa. This drug protein is known as Anakinra, and has an effective application in the treatment of rheumatoid arthritis. This study was conducted to examine the produce of the recombinant IL-1RA protein in Escherichia coli (E. coli) strains.
Methods: Codon optimization of IL-1RA gene was done using GenScript, and the gene was cloned in the pUC18 as cloning vector. Then, plasmid was cut by two restriction enzymes including NdeI and BamH1 enzymes. IL-1RA gene was purified from the agarose gel. IL-1RA gene was ligated into expression vector. The constructed expression cassette was transformed into E. coli BL21 (DE3) Origami (DE3) and Rosetta (DE3) using CaCl2 and heat shock method.
Findings: Identification and confirmation of transformed colonies was performed using colony polymerase chain reaction (PCR). Induction of this gene was done with isopropyl β- d-1-thiogalactopyranoside (IPTG). The protein expression was analyzed using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and western blotting techniques, and it purified by Ni nickel resin. Expression analysis of transformed E. coli strains confirmed that gene integrated into expression host. Molecular weight of expressed protein was estimated to be 16.83 kDa.
Conclusion: In this study, Human IL-1RA was successfully produced in E. coli Origami with high quantity other than the rest of E. coli strains. Therefore, E. coli BL21 Origami (DE3) can be used as the suitable host for production of recombinant IL-1RA, and this technology has a potential for localization. |
| format | Article |
| id | doaj-art-c67befcd015b4c0d936c8ce3f36d2b95 |
| institution | Directory of Open Access Journals |
| issn | 1027-7595 1735-854X |
| language | fas |
| publishDate | 2019-11-01 |
| publisher | Isfahan University of Medical Sciences |
| record_format | Article |
| spelling | doaj-art-c67befcd015b4c0d936c8ce3f36d2b952025-08-19T22:31:52ZfasIsfahan University of Medical Sciencesمجله دانشکده پزشکی اصفهان1027-75951735-854X2019-11-013753996597210.22122/jims.v37i539.122293482Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3)Hanieh Fardgoli0Seyed Nezameddin Hoseini1Setareh Haghighat2MSc Student, Department of Microbiology, School of Advanced Science and Technology, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, IranAssociate Professor, Department of Recombinant Hepatitis B Vaccine, Production and Research Complex, Pasteur Institute of Iran, IranAssistant Professor, Department of Microbiology, School of Advanced Science and Technology, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, IranBackground: Recombinant human interleukin-1 receptor antagonist (IL-1RA) is a protein with 153 amino acids and molecular weight of 16.83 kDa. This drug protein is known as Anakinra, and has an effective application in the treatment of rheumatoid arthritis. This study was conducted to examine the produce of the recombinant IL-1RA protein in Escherichia coli (E. coli) strains. Methods: Codon optimization of IL-1RA gene was done using GenScript, and the gene was cloned in the pUC18 as cloning vector. Then, plasmid was cut by two restriction enzymes including NdeI and BamH1 enzymes. IL-1RA gene was purified from the agarose gel. IL-1RA gene was ligated into expression vector. The constructed expression cassette was transformed into E. coli BL21 (DE3) Origami (DE3) and Rosetta (DE3) using CaCl2 and heat shock method. Findings: Identification and confirmation of transformed colonies was performed using colony polymerase chain reaction (PCR). Induction of this gene was done with isopropyl β- d-1-thiogalactopyranoside (IPTG). The protein expression was analyzed using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and western blotting techniques, and it purified by Ni nickel resin. Expression analysis of transformed E. coli strains confirmed that gene integrated into expression host. Molecular weight of expressed protein was estimated to be 16.83 kDa. Conclusion: In this study, Human IL-1RA was successfully produced in E. coli Origami with high quantity other than the rest of E. coli strains. Therefore, E. coli BL21 Origami (DE3) can be used as the suitable host for production of recombinant IL-1RA, and this technology has a potential for localization.http://jims.mui.ac.ir/index.php/jims/article/view/12229interleukin 1 receptor antagonist proteinrecombinationescherichia coli |
| spellingShingle | Hanieh Fardgoli Seyed Nezameddin Hoseini Setareh Haghighat Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3) interleukin 1 receptor antagonist protein recombination escherichia coli |
| title | Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3) |
| title_full | Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3) |
| title_fullStr | Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3) |
| title_full_unstemmed | Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3) |
| title_short | Cloning and Expression of Recombinant Human Interleukin 1 Receptor Antagonist in Escherichia Coli Strains, BL21 (DE3), Rosetta (DE3), and Origami (DE3) |
| title_sort | cloning and expression of recombinant human interleukin 1 receptor antagonist in escherichia coli strains bl21 de3 rosetta de3 and origami de3 |
| topic | interleukin 1 receptor antagonist protein recombination escherichia coli |
| url | http://jims.mui.ac.ir/index.php/jims/article/view/12229 |
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