Expression, purification and characterisation of recombinant Escherichia coli derived chicken interleukin-12

Vet Immunol Immunopathol. 2008 Dec 15;126(3-4):403-6. doi: 10.1016/j.vetimm.2008.08.004. Epub 2008 Aug 23.

Abstract

Zoonotic viruses, such as H5N1 Avian Influenza, pose major threats to both animals and humans, and with this in mind there is a need for the development of new anti-viral strategies. The cytokine interleukin-12 (IL-12) is known to play a pivotal regulatory role in the anti-viral response due to its role in the induction of the key anti-viral cytokine IFN-gamma. Therefore, strategies which provide a means for the production of therapeutic quantities of IL-12 may be of major benefit. Here we describe the development of biologically active Escherichia coli (E. coli) derived chicken IL-12 (ChIL-12). The single chain ChIL-12 gene was cloned into the pET32b expression vector, transformed into the BL-21 E. coli strain and expression induced with IPTG. Over expressed protein was solubilised with zwittergent detergent and isolated utilising Nickel ion affinity chromatography. Biological activity was determined as ChIL-12 stimulated proliferation of pre-treated T-cells in vitro. This study is the first example of a biologically active E. coli derived IL-12 from a non-mammalian vertebrate subsequently providing a means for testing the anti-viral therapeutic potential of ChIL-12 in an in vivo model.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chickens / genetics*
  • Chickens / immunology
  • Chromatography, Affinity
  • Cloning, Molecular
  • Escherichia coli
  • Genetic Vectors / genetics*
  • Interleukin-12 / genetics*
  • Interleukin-12 / metabolism*
  • Isopropyl Thiogalactoside

Substances

  • Interleukin-12
  • Isopropyl Thiogalactoside