Structural highlights
Function
[SPB3_HUMAN] May act as a protease inhibitor to modulate the host immune response against tumor cells.
Publication Abstract from PubMed
Psoriasis is a chronic inflammatory skin disease. The absence of microbial organisms as potential causal agents has given rise to the hypothesis that the inflammation is due to an autoimmune reaction. The defined inflamed areas of the skin lesions argue for an immunological disease with a local production of a causal antigen. Pso p27 is a protein generated in mast cells in psoriatic plaques, but not in uninvolved skin. We recently demonstrated that the Pso p27 is generated by cleavage of SerpinB3 (SCCA1) in the presence of mast cell associated chymase. In this communication we demonstrate by X-ray crystallographic analysis that the cleavage products associate into a complex similar to SCCA1, but with the reactive centre loop inserted into a 5-stranded central beta-sheet. Native gel electrophoresis show that these Pso p27 complexes form large aggregates which may be of significance with respect to an immunogenic role of Pso p27.
Psoriasis pathogenesis - Pso p27 constitutes a compact structure forming large aggregates.,Lysvand H, Helland R, Hagen L, Slupphaug G, Iversen OJ Biochem Biophys Rep. 2015 Jun 9;2:132-136. doi: 10.1016/j.bbrep.2015.06.001., eCollection 2015 Jul. PMID:29124154[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Lysvand H, Helland R, Hagen L, Slupphaug G, Iversen OJ. Psoriasis pathogenesis - Pso p27 constitutes a compact structure forming large aggregates. Biochem Biophys Rep. 2015 Jun 9;2:132-136. doi: 10.1016/j.bbrep.2015.06.001., eCollection 2015 Jul. PMID:29124154 doi:https://dx.doi.org/10.1016/j.bbrep.2015.06.001
