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4DKE

Crystal Structure of Human Interleukin-34 Bound to FAb1.1

Summary for 4DKE
Entry DOI10.2210/pdb4dke/pdb
Related4dkc 4dkd 4dkf
DescriptorInterleukin-34, FAb1.1 Heavy Chain, FAb1.1 Light Chain, ... (6 entities in total)
Functional Keywordsdimeric four-helix bundle cytokine, igg, glycosylation, cytokine-immune system complex, cytokine/immune system
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight141041.80
Authors
Ma, X.,Chen, Y.,Stawicki, S.,Wu, Y.,Bazan, J.F.,Starovasnik, M.A. (deposition date: 2012-02-03, release date: 2012-04-11, Last modification date: 2024-11-27)
Primary citationMa, 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: 22483114
DOI: 10.1016/j.str.2012.02.010
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3 Å)
Structure validation

231029

数据于2025-02-05公开中

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