The modular serine proteases of the complement cascade

被引:43
作者
Forneris, Federico [1 ]
Wu, Jin [1 ]
Gros, Piet [1 ]
机构
[1] Univ Utrecht, Dept Chem, Fac Sci, Bijvoet Ctr Biomol Res, NL-3584 CH Utrecht, Netherlands
基金
欧洲研究理事会;
关键词
MEMBRANE COFACTOR PROTEIN; MANNAN-BINDING LECTIN; VENOM FACTOR COMPLEX; FACTOR-H; C1; INHIBITOR; FACTOR-B; CRYSTAL-STRUCTURE; CATALYTIC DOMAIN; STRUCTURAL BASIS; 1ST COMPONENT;
D O I
10.1016/j.sbi.2012.04.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Modular serine proteases are central to the complement cascade of the mammalian humoral immune system. These proteases form protein complexes through multi-domain interactions to achieve their proteolytic activity. We review the structural insights into complement initiation by auto-activation of the hetero-tetrameric proteases of the large danger-recognition protein complexes, amplification and labelling of particles by the formation and activity of C3 convertases, and regulation by convertase dissociation and degradation to prevent 'bystander' damage to healthy host cells and tissues. The data reveal that complex formation and large domain-domain rearrangements underlie the proteolytic reactions of the complement cascade, which enables the host to recognize and clear invading microbes and host debris from its blood and fluids surrounding tissues.
引用
收藏
页码:333 / 341
页数:9
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