4.5 Article

Crystal structure of a soluble decoy receptor IL-22BP bound to interleukin-22

Journal

FEBS LETTERS
Volume 583, Issue 7, Pages 1072-1077

Publisher

WILEY
DOI: 10.1016/j.febslet.2009.03.006

Keywords

Cytokine; IL-22; IL-22BP; Interleukin; Immunology; X-ray crystallography

Funding

  1. FAPESP [06/00182-8, 06/01534-5]
  2. CNPq [154559/2006-7]
  3. Fonds National de la Recherche Scientifique, Belgium.
  4. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [06/01534-5, 06/00182-8] Funding Source: FAPESP

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Interleukin-22 (IL-22) plays an important role in the regulation of immune and inflammatory responses in mammals. The IL-22 binding protein (IL-22BP), a soluble receptor that specifically binds IL-22, prevents the IL-22/interleukin-22 receptor 1 (IL-22R1)/interleukin-10 receptor 2 (IL-10R2) complex assembly and blocks IL-22 biological activity. Here we present the crystal structure of the IL-22/IL-22BP complex at 2.75 angstrom resolution. The structure reveals IL-22BP residues critical for IL-22 binding, which were confirmed by site-directed mutagenesis and functional studies. Comparison of IL-22/IL-22BP and IL-22/IL-22R1 crystal structures shows that both receptors display an overlapping IL-22 binding surface, which is consistent with the inhibitory role played by IL-22 binding protein.

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