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Abstract

Response Surface Optimization of the Expression Conditions for Synthetic Human Interferon alpha-2b Gene in Escherichia coli

Author(s): Z. Eslami Samarin, S. Abolghasemi , E. Dehnavi , A. Akbarzadeh , A. Hadian , M. Khodabandeh, M. Aghaeepoor
Department of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Gene Transfer Pioneers (GTP) Research Group, Shahid Beheshti University of Medical Sciences, Department of Marine Biology, Science and Research Branch, Islamic Azad University, Tehran, Semnan Biotechnology Research Center, Semnan University of Medical Sciences, Semnan, Iran

Correspondence Address:
Semnan Biotechnology Research Center, Semnan University of Medical Sciences, Semnan, Iran, E-mail: [email protected]


Recombinant human interferon alpha-2b is an FDA-approved drug for monotherapy or in combination therapy with other drugs for hepatitis and cancers. It belongs to a family of homologous proteins involved in antiviral, antiproliferative, and immunoregulatory processes. A different expression system has been used for overexpression of this protein. Escherichia coli expression system is a highly characterized host and various expression settings have been developed based on its properties. However, finding the best conditions for the overexpression of recombinant human interferon alpha-2b remains to be addressed. In this study, the expression of synthetic human interferon alpha-2b gene in E. coli was greatly improved by adjusting the expression condition. In this regard, a recombinant gene was designed and codon optimized for the periplasmic expression of this protein. Then, gene subcloning was employed to insert the synthesized gene into the pET22b expression vector. Thereafter, the response surface methodology method was employed to design 20 experiments to find out the optimum points for isopropyl β-D-1-thiogalactopyranoside concentration, post-induction period, and the cell density of induction (OD600). The expression fluctuations were assessed by using the real time polymerase chain reaction method. Our results indicated that the synthetic human interferon alpha-2b gene was successfully codon optimized and subcloned into the expression vector. The real time polymerase chain reaction results revealed that the optimum levels of the selected parameters are 0.27 mM for isopropyl β-D-1-thiogalactopyranoside concentration, 7.98 H for the post-induction period, and 3.93 for cell density (OD600). These optimized conditions led to a 3.5-fold increase in the rhIFNα2b expression, which is highly promising for large scale rhIFNα2b overexpression.

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