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4ADQ

CRYSTAL STRUCTURE OF THE MOUSE COLONY-STIMULATING FACTOR 1 (MCSF-1) CYTOKINE IN COMPLEX WITH THE VIRAL RECEPTOR BARF1

Summary for 4ADQ
Entry DOI10.2210/pdb4adq/pdb
Related4ADF
DescriptorSECRETED PROTEIN BARF1, MACROPHAGE COLONY-STIMULATING FACTOR 1, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
Functional Keywordsimmune system-receptor complex, rtkiii, extracellular, cytokine receptor-cytokine complex, four-helix bundle, glycoprotein, immunoglobulin domain, oncogene, cytokine/signaling, immune system/receptor
Biological sourceHuman gammaherpesvirus 4
More
Total number of polymer chains8
Total formula weight167647.35
Authors
Elegheert, J.,Bracke, N.,Savvides, S.N. (deposition date: 2012-01-02, release date: 2012-08-22, Last modification date: 2024-10-16)
Primary citationElegheert, J.,Bracke, N.,Pouliot, P.,Gutsche, I.,Shkumatov, A.V.,Tarbouriech, N.,Verstraete, K.,Bekaert, A.,Burmeister, W.P.,Svergun, D.I.,Lambrecht, B.N.,Vergauwen, B.,Savvides, S.N.
Allosteric Competitive Inactivation of Hematopoietic Csf-1 Signaling by the Viral Decoy Receptor Barf1.
Nat.Struct.Mol.Biol., 19:938-, 2012
Cited by
PubMed Abstract: Hematopoietic human colony-stimulating factor 1 (hCSF-1) is essential for innate and adaptive immunity against viral and microbial infections and cancer. The human pathogen Epstein-Barr virus secretes the lytic-cycle protein BARF1 that neutralizes hCSF-1 to achieve immunomodulation. Here we show that BARF1 binds the dimer interface of hCSF-1 with picomolar affinity, away from the cognate receptor-binding site, to establish a long-lived complex featuring three hCSF-1 at the periphery of the BARF1 toroid. BARF1 locks dimeric hCSF-1 into an inactive conformation, rendering it unable to signal via its cognate receptor on human monocytes. This reveals a new functional role for hCSF-1 cooperativity in signaling. We propose a new viral strategy paradigm featuring an allosteric decoy receptor of the competitive type, which couples efficient sequestration and inactivation of the host growth factor to abrogate cooperative assembly of the cognate signaling complex.
PubMed: 22902366
DOI: 10.1038/NSMB.2367
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (4.5 Å)
Structure validation

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