1. Academic Validation
  2. Heterologous expression, immunochemical and computational analysis of recombinant human interferon alpha 2b

Heterologous expression, immunochemical and computational analysis of recombinant human interferon alpha 2b

  • Springerplus. 2013 Jun 15;2(1):264. doi: 10.1186/2193-1801-2-264.
Iram Gull 1 Zahoor Qadir Samra Muhammad Shahbaz Aslam Muhammad Amin Athar
Affiliations

Affiliation

  • 1 Institute of Biochemistry and Biotechnology, University of the Punjab, Quaid-i-Azam Campus, Lahore, 54590 Pakistan.
Abstract

Interferon alpha 2b (IFNα-2b) is an important cytokine and used for Antiviral and Anticancer treatment. The low cost production of IFNα-2b with high biological activity is necessary to provide the interferon therapy to the hepatitis patients in Pakistan. In the present study, human interferon alpha 2b (hIFNα-2b) gene from a healthy person was cloned and overexpressed in E. coli BL21(DE3). The molecular weight of the expressed hIFNα-2b is 19 kDa. The over expressed recombinant hIFNα-2b was checked by ELISA using Antibodies raised against commercially available hIFNα-2b. The biocomputational analysis of recombinant hIFNα-2b gene showed the 99.9% nucleotide sequence and 100% deduced amino acid sequence homology with reported sequences of IFNα-2b. The predicted 3D-structure showed mainly five α-helices, one 310 helix and two disulfide bonds at Cys1-Cys98 and Cys129-Cys138. The amino acid sequence alignment indicated that the disulfide linkage position is conserved in all IFNα family members. On the basis of sequence homology among interferon alpha family, new potent variants of hIFNα-2b with enhance efficacy can be produced. Indigenous production of IFNα-2b from gene of local population will reduce the cost and increase tolerability of interferon therapy.

Keywords

Cloning; Computational analysis; Overexpression; hIFNα-2b.

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