Document Type
Article
Publication Date
Spring 2-23-2012
Abstract
Activation of the complement system results in formation of membrane attack complexes (MACs), pores that disrupt lipid bilayers and lyse bacteria and other pathogens. Here, we present the crystal structure of the first assembly intermediate, C5b6, together with a cryo-electron microscopy reconstruction of a soluble, regulated form of the pore, sC5b9. Cleavage of C5 to C5b results in marked conformational changes, distinct from those observed in the homologous C3-to-C3b transition. C6 captures this conformation, which is preserved in the larger sC5b9 assembly. Together with antibody labeling, these structures reveal that complement components associate through sideways alignment of the central MAC-perforin (MACPF) domains, resulting in a C5b6-C7-C8β-C8α-C9 arc. Soluble regulatory proteins below the arc indicate a potential dual mechanism in protection from pore formation. These results provide a structural framework for understanding MAC pore formation and regulation, processes important for fighting infections and preventing complement-mediated tissue damage.
Persistant Identifier
http://hdl.handle.net/10950/4541
Publisher
ScienceDirect
Permanent Email Address
archivist@uttyler.edu
Recommended Citation
Hadders, Michael A.; Bubeck, Doryen; Roversi, Pietro; Hakobyan, Svetlana; Forneris, Federico; Morgan, B. Paul; Pangburn, Michael K.; Llorca, Oscar; Lea, Susan M.; and Gros, Piet, "Assembly and Regulation of the Membrane Attack Complex Based on Structures of C5b6 and sC5b9" (2012). School of Medicine Faculty Publications and Presentations. Paper 3.
Description
This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (CC-BY; http:// creativecommons.org/licenses/by/3.0/legalcode).