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Title: Engineered acid-stabile human interferon gamma. Author: Kontsek P, Waschütza G, Kontseková E, Otto B. Journal: Cytokine; 2000 Jun; 12(6):708-10. PubMed ID: 10843749. Abstract: Loss of anti-viral potency upon pH2-treatment is an inherent feature of interferon (IFN)-gamma. The phenomenon seems to be caused by dissociation of IFN-gamma homodimer into subunits upon acidification and subsequent self-association of monomers into aggregates with reduced activity after neutralization. We demonstrated that acid-stability could be engineered into human IFN-gamma without affecting its specific activity. An artificial intra-monomer disulphide bond E7C/S69C stabilizes the dimeric form of the cytokine, which retained its full bioactivity after exposure to pH2. Acidification did not modify the antigenic structure of IFN-gamma as proved by a panel of mouse anti-human IFNgamma antibodies.[Abstract] [Full Text] [Related] [New Search]