Purification, cloning, expression and biological characterization of an interleukin-1 receptor antagonist protein
Copyright policy )Purification, cloning, expression and biological characterization of an interleukin-1 receptor antagonist protein
A human myelomonocytic cell line, U937, produced an interleukin-1 (IL-1) receptor antagonist protein (IRAP) which was purified and partially sequenced. A complementary DNA coding for IRAP was cloned and sequenced. The mature translation product of the cDNA has been expressed in Escherichia coli and was an active competitive inhibitor of the binding of IL-1 to the T-cell/fibroblast form of the IL-1 receptor. Recombinant IRAP specifically inhibited IL-1 bioactivity on T cells and endothelial cells in vitro and was a potent inhibitor of IL-1 induced corticosterone production in vivo.
- Upjohn United States
Base Sequence, Molecular Sequence Data, Gene Expression, Granulocyte-Macrophage Colony-Stimulating Factor, DNA, Binding, Competitive, Monocytes, Cell Line, Interleukin 1 Receptor Antagonist Protein, Mice, Colony-Stimulating Factors, Cell Adhesion, Animals, Humans, Amino Acid Sequence, Cloning, Molecular, Corticosterone, Growth Substances, Granulocytes, Interleukin-1
Base Sequence, Molecular Sequence Data, Gene Expression, Granulocyte-Macrophage Colony-Stimulating Factor, DNA, Binding, Competitive, Monocytes, Cell Line, Interleukin 1 Receptor Antagonist Protein, Mice, Colony-Stimulating Factors, Cell Adhesion, Animals, Humans, Amino Acid Sequence, Cloning, Molecular, Corticosterone, Growth Substances, Granulocytes, Interleukin-1
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