The mystery behind membrane insertion: a review of the complement membrane attack complex

被引:112
作者
Bayly-Jones, Charles [1 ,2 ]
Bubeck, Doryen [3 ]
Dunstone, Michelle A. [1 ,2 ]
机构
[1] Monash Univ, Biomed Discovery Inst, Dept Biochem & Mol Biol, Clayton Campus, Melbourne, Vic 3800, Australia
[2] Monash Univ, Biomed Discovery Inst, ARC Ctr Excellence Adv Mol Imaging, Clayton Campus, Melbourne, Vic 3800, Australia
[3] Imperial Coll London, Dept Life Sci, South Kensington Campus, London SW2 7AZ, England
基金
澳大利亚国家健康与医学研究理事会;
关键词
membrane attack complex; MACPF; pore-forming protein; pore-forming toxins; cholesterol-dependent cytolysin; complement pathway; CHOLESTEROL-DEPENDENT CYTOLYSIN; PORE-FORMING TOXIN; STRUCTURAL BASIS; REGULATORY PROTEINS; CRYSTAL-STRUCTURE; 9TH COMPONENT; ESCHERICHIA-COLI; SOMATIC MUTATION; PERFRINGOLYSIN-O; BINDING-SITES;
D O I
10.1098/rstb.2016.0221
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The membrane attack complex (MAC) is an important innate immune effector of the complement terminal pathway that forms cytotoxic pores on the surface of microbes. Despite many years of research, MAC structure and mechanism of action have remained elusive, relying heavily on modelling and inference from biochemical experiments. Recent advances in structural biology, specifically cryo-electron microscopy, have provided new insights into the molecular mechanism of MAC assembly. Its unique 'split-washer' shape, coupled with an irregular giant beta-barrel architecture, enable an atypical mechanism of hole punching and represent a novel system for which to study pore formation. This review will introduce the complement terminal pathway that leads to formation of the MAC. Moreover, it will discuss how structures of the pore and component proteins underpin a mechanism for MAC function, modulation and inhibition.
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页数:9
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