Printed in Great Britain Purification of Human Fibroblast Interferon by Zinc Chelate Chromatography

Human interferon was prepared by superinduction of cultures of either diploid embryonic skin and muscle cells or of the osteosarcoma; cell line MG-63. The interferon so btained was concentrated and partially purified by adsorption to controlled pore glass (CPG) beads at neutral pH and deso~ption by glycine-HC1 buffer at pH 2. After neutralization, this interferon was applied to a column of zinc chelate which was eluted withbuffers of decreasing pH. Most of the proteins eluted ahead of the interferon activity, which itself eluted in two distinct peaks. The first peak occurred in the effluent fractions around pH 5.9, and the second one in fractions around pH 5.2. The interferon found in fractions of pH 5.9 contained 5 % of the original contaminating proteins. In contrast, he amount of total protein in the pH 5.2 peak was so small that it could not accurately be assayed by the fluorescamine method. Consequently, the interferon in the peak fraction was estimated to have a specific activity of about 2 × 109 units/rag. This material was radiolabelled and analysed by electrophoresis. A major peak of about 22000 mol. wt. with only minor contaminating proteins appeared on the autoradiographs. The total recovery of the zinc chelate chromatographical procedure was nearly 100%, and the interferon recovered from each peak behaved consistently on rechromatography. Fibroblast interferon produced by most diploid cells contained less than 10 % of the variant eluting at pH 5.9. MG-63 cells and high-passage cultures of some diploid cell strains produced up to 50 % of this variant