2icf
From Proteopedia
Line 1: | Line 1: | ||
[[Image:2icf.gif|left|200px]] | [[Image:2icf.gif|left|200px]] | ||
- | + | <!-- | |
- | + | The line below this paragraph, containing "STRUCTURE_2icf", creates the "Structure Box" on the page. | |
- | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
- | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
- | | | + | or leave the SCENE parameter empty for the default display. |
- | | | + | --> |
- | + | {{STRUCTURE_2icf| PDB=2icf | SCENE= }} | |
- | + | ||
- | + | ||
- | }} | + | |
'''CRIg bound to C3b''' | '''CRIg bound to C3b''' | ||
Line 26: | Line 23: | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
[[Category: Wiesmann, C.]] | [[Category: Wiesmann, C.]] | ||
- | [[Category: | + | [[Category: Alternate pathway]] |
- | [[Category: | + | [[Category: C3]] |
- | [[Category: | + | [[Category: C3b]] |
- | [[Category: | + | [[Category: Complement]] |
- | [[Category: | + | [[Category: Complement receptor]] |
- | [[Category: | + | [[Category: Crig]] |
- | [[Category: | + | [[Category: Immune system]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 07:19:47 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 04:19, 4 May 2008
CRIg bound to C3b
Overview
The complement system is a key part of the innate immune system, and is required for clearance of pathogens from the bloodstream. After exposure to pathogens, the third component of the complement system, C3, is cleaved to C3b which, after recruitment of factor B, initiates formation of the alternative pathway convertases. CRIg, a complement receptor expressed on macrophages, binds to C3b and iC3b mediating phagocytosis of the particles, but it is unknown how CRIg selectively recognizes proteolytic C3-fragments and whether binding of CRIg to C3b inhibits convertase activation. Here we present the crystal structure of C3b in complex with CRIg and, using CRIg mutants, provide evidence that CRIg acts as an inhibitor of the alternative pathway of complement. The structure shows that activation of C3 induces major structural rearrangements, including a dramatic movement (>80 A) of the thioester-bond-containing domain through which C3b attaches to pathogen surfaces. We show that CRIg is not only a phagocytic receptor, but also a potent inhibitor of the alternative pathway convertases. The structure provides insights into the complex macromolecular structural rearrangements that occur during complement activation and inhibition. Moreover, our structure-function studies relating the structural basis of complement activation and the means by which CRIg inhibits the convertases provide important clues to the development of therapeutics that target complement.
About this Structure
2ICF is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Structure of C3b in complex with CRIg gives insights into regulation of complement activation., Wiesmann C, Katschke KJ, Yin J, Helmy KY, Steffek M, Fairbrother WJ, McCallum SA, Embuscado L, DeForge L, Hass PE, van Lookeren Campagne M, Nature. 2006 Nov 9;444(7116):217-20. Epub 2006 Oct 15. PMID:17051150 Page seeded by OCA on Sun May 4 07:19:47 2008