4DKC
Crystal Structure of Human Interleukin-34
Summary for 4DKC
Entry DOI | 10.2210/pdb4dkc/pdb |
Related | 4DKD 4DKe 4DKf |
Descriptor | Interleukin-34, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose (3 entities in total) |
Functional Keywords | dimeric four-helix bundle cytokine, activating csf-1r, csf-1 receptor, glycosylation, n76, cytokine |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 2 |
Total formula weight | 44894.78 |
Authors | Ma, X.,Bazan, J.F.,Starovasnik, M.A. (deposition date: 2012-02-03, release date: 2012-04-11, Last modification date: 2024-10-09) |
Primary citation | Ma, X.,Lin, W.Y.,Chen, Y.,Stawicki, S.,Mukhyala, K.,Wu, Y.,Martin, F.,Bazan, J.F.,Starovasnik, M.A. Structural Basis for the Dual Recognition of Helical Cytokines IL-34 and CSF-1 by CSF-1R. Structure, 20:676-687, 2012 Cited by PubMed Abstract: Lacking any discernible sequence similarity, interleukin-34 (IL-34) and colony stimulating factor 1 (CSF-1) signal through a common receptor CSF-1R on cells of mononuclear phagocyte lineage. Here, the crystal structure of dimeric IL-34 reveals a helical cytokine fold homologous to CSF-1, and we further show that the complex architecture of IL-34 bound to the N-terminal immunoglobulin domains of CSF-1R is similar to the CSF-1/CSF-1R assembly. However, unique conformational adaptations in the receptor domain geometry and intermolecular interface explain the cross-reactivity of CSF-1R for two such distantly related ligands. The docking adaptations of the IL-34 and CSF-1 quaternary complexes, when compared to the stem cell factor assembly, draw a common evolutionary theme for transmembrane signaling. In addition, the structure of IL-34 engaged by a Fab fragment reveals the mechanism of a neutralizing antibody that can help deconvolute IL-34 from CSF-1 biology, with implications for therapeutic intervention in diseases with myeloid pathogenic mechanisms. PubMed: 22483114DOI: 10.1016/j.str.2012.02.010 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.85 Å) |
Structure validation
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