2pnd
From Proteopedia
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Structure or murine CRIg
Overview
Complement is an important component of the innate and adaptive immune, response, yet complement split products generated through activation of, each of the three complement pathways (classical, alternative, and lectin), can cause inflammation and tissue destruction. Previous studies have shown, that complement activation through the alternative, but not classical, pathway is required to initiate antibody-induced arthritis in mice, but it, is unclear if the alternative pathway (AP) plays a role in established, disease. Previously, we have shown that human complement receptor of the, immunoglobulin superfamily (CRIg) is a selective inhibitor of the AP of, complement. Here, we present the crystal structure of murine CRIg and, using mutants, provide evidence that the structural requirements for, inhibition of the AP are conserved in human and mouse. A soluble form of, CRIg reversed inflammation and bone loss in two experimental models of, arthritis by inhibiting the AP of complement in the joint. Our data, indicate that the AP of complement is not only required for disease, induction, but also disease progression. The extracellular domain of CRIg, thus provides a novel tool to study the effects of inhibiting the AP of, complement in established disease and constitutes a promising therapeutic, with selectivity for a single complement pathway.
About this Structure
2PND is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.
Reference
A novel inhibitor of the alternative pathway of complement reverses inflammation and bone destruction in experimental arthritis., Katschke KJ Jr, Helmy KY, Steffek M, Xi H, Yin J, Lee WP, Gribling P, Barck KH, Carano RA, Taylor RE, Rangell L, Diehl L, Hass PE, Wiesmann C, van Lookerenb Campagne M, J Exp Med. 2007 Jun 11;204(6):1319-25. Epub 2007 Jun 4. PMID:17548523
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