摘要

We developed a technique for production of human interferon-alpha 2a (IFN-alpha 2a) and IFN-alpha 2b lacking the N-terminal methionine. First of all, we constructed plasmids containing genes of hybrid IFN-alpha 2 controlled by different promoters; the proximal part of the genes incorporated various sequences encoding the enteropeptidase cleavage site. As a result, four strains of Escherichia coli producing hybrid IFN-alpha 2 were obtained. The protocol for IFN-alpha 2 renaturation, cleavege of its N-terminal part, and chromatographic purification of the N-terminal methionine-free IFN-alpha 2 was developed.

  • 出版日期2011-6

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