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    EMBO J. 2000 Jul 17;19(14):3530-41.

    Charged residues dominate a unique interlocking topography in the heterodimeric cytokine interleukin-12.

    Yoon C, Johnston SC, Tang J, Stahl M, Tobin JF, Somers WS.

    Departments of Musculoskeletal Sciences and Biological Chemistry, Wyeth Research, 87 Cambridge Park Drive, Cambridge, MA 02140, USA.

    Human interleukin-12 (IL-12, p70) is an early pro-inflammatory cytokine, comprising two disulfide-linked subunits, p35 and p40. We solved the crystal structures of monomeric human p40 at 2.5 A and the human p70 complex at 2.8 A resolution, which reveals that IL-12 is similar to class 1 cytokine-receptor complexes. They also include the first description of an N-terminal immunoglobulin-like domain, found on the p40 subunit. Several charged residues from p35 and p40 intercalate to form a unique interlocking topography, shown by mutagenesis to be critical for p70 formation. A central arginine residue from p35 projects into a deep pocket on p40, which may be an ideal target for a small molecule antagonist of IL-12 formation.

    PMID: 10899108 [PubMed - indexed for MEDLINE]

    PMCID: 313992

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