پنجشنبه 4 اردیبهشت 1404
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دوره 32، شماره 155 - ( 8-1403 )
جلد 32 شماره 155 صفحات 488-477 |
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Ethics code: IR.ZUMS.REC.1400.030
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Shamsi S, Mahdei Nasirmahalleh N, Shirmohammadpour M, Afshar D, Mirzaei B. Design, Cloning, and Expression of PLC-Darpin Fusion Protein as Putative Immunotoxin in a Prokaryotic Host. J Adv Med Biomed Res 2024; 32 (155) :477-488
URL: http://journal.zums.ac.ir/article-1-7563-fa.html
URL: http://journal.zums.ac.ir/article-1-7563-fa.html
Design, Cloning, and Expression of PLC-Darpin Fusion Protein as Putative Immunotoxin in a Prokaryotic Host. Journal of Advances in Medical and Biomedical Research. 1403; 32 (155) :477-488
چکیده: (204 مشاهده)
Background & Objective: Cancers are common genetic disease that can cause death. Bacteria, such as Clostridium novyi, potentially could be used in cancer treatment by producing an enzyme called phospholipase C (PLC), which causes cell lysis. The aims of this study are to cloning and expression of PLC- Darpin in prokaryotic host.
Materials & Methods: Briefly, the PLC- Darpin gene sequence was amplified using PCR. The amplified fragment was conducted into the pET28a vector, transformed into E. coli BL21 (DE3), and screened by the double digestion method. Protein expression was analyzed using SDS-PAGE and checked with specific antibodies using the western blotting method. The cloned fragment was confirmed using the PCR colony method.
Results: Designed PLC- Darpin protein sequence (1600 bp) was successfully amplified by specific primers taking advantage of PCR method. Then, cloned PLC- Darpin candidate sequence was reconfirmed by digestion procedure, and colony PCR. Finally, 60 KDa expressed protein in prokaryotic host reconfirmed by SDS- page and western blotting.
Conclusion: Fused PLC enzyme to Darpin protein could be considered as a main putative immunotoxin due to its enzymatic role and cytotoxicity which may be utilized as a therapeutic choice in the future with further investigations.
Materials & Methods: Briefly, the PLC- Darpin gene sequence was amplified using PCR. The amplified fragment was conducted into the pET28a vector, transformed into E. coli BL21 (DE3), and screened by the double digestion method. Protein expression was analyzed using SDS-PAGE and checked with specific antibodies using the western blotting method. The cloned fragment was confirmed using the PCR colony method.
Results: Designed PLC- Darpin protein sequence (1600 bp) was successfully amplified by specific primers taking advantage of PCR method. Then, cloned PLC- Darpin candidate sequence was reconfirmed by digestion procedure, and colony PCR. Finally, 60 KDa expressed protein in prokaryotic host reconfirmed by SDS- page and western blotting.
Conclusion: Fused PLC enzyme to Darpin protein could be considered as a main putative immunotoxin due to its enzymatic role and cytotoxicity which may be utilized as a therapeutic choice in the future with further investigations.
نوع مطالعه: مقاله پژوهشی |
موضوع مقاله:
Life Science
دریافت: 1403/6/18 | پذیرش: 1403/11/25 | انتشار: 1403/7/19
دریافت: 1403/6/18 | پذیرش: 1403/11/25 | انتشار: 1403/7/19
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