Title of article :
Expression Optimization of Anti-CD22 scFv-Apoptin Fusion Protein Using Experimental Design Methodology
Author/Authors :
Shahhosseini, Soraya Department of Pharmaceutical Chemistry - School of Pharmacy - Shahid Beheshti University of Medical Sciences - Tehran, Iran , Agha Amiri, Solmaz Department of Pharmaceutical Biotechnology - School of Pharmacy - Shahid Beheshti University of Medical Sciences - Tehran, Iran , Zarei, Najmeh Department of Medical Biotechnolgy - Biotechnology Research Center - Pasteur Institute of Iran - Tehran, Iran , Enayati, Somayeh Department of Medical Biotechnolgy - Biotechnology Research Center - Pasteur Institute of Iran - Tehran, Iran , Azizi,Mohammad Department of Medical Biotechnolgy - Biotechnology Research Center - Pasteur Institute of Iran - Tehran, Iran , Khalaj, Vahid Department of Medical Biotechnolgy - Biotechnology Research Center - Pasteur Institute of Iran - Tehran, Iran
Pages :
4
From page :
66
To page :
69
Abstract :
Design of experiments is a rapid and cost-effective approach for optimization of recombinant protein production process. In our previous study, we generated a potent dual-acting fusion protein, anti-CD22 scFv-apoptin, to target B-cell malignant cell lines. In the present investigation, we report the effect of different variables on the expression levels of this fusion protein. Methods: Four variables (cell optical density at induction, IPTG concentration, induction temperature, and induction time) were tested using experimental design. Results: Our findings demonstrated that among the examined variables, only the induction time had a significant positive effect on the protein expression yield. Conclusion: Experimental design was successfully applied in this study. The optimized condition obtained in the current study can be applied in future commercial production of this novel fusion protein.
Keywords :
E. coli , Fusion proteins , Single-chain antibodies , Recombinant protein
Journal title :
Astroparticle Physics
Serial Year :
2018
Record number :
2480156
Link To Document :
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