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膜攻击复合物的结构生物学

Structural biology of the membrane attack complex.

作者信息

Sonnen Andreas F-P, Henneke Philipp

机构信息

Center for Chronic Immunodeficiency, University Medical Center Freiburg, Breisacher Straße 117, 79106, Freiburg, Germany,

出版信息

Subcell Biochem. 2014;80:83-116. doi: 10.1007/978-94-017-8881-6_6.

Abstract

The complement system is an intricate network of serum proteins that mediates humoral innate immunity through an amplification cascade that ultimately leads to recruitment of inflammatory cells or opsonisation or killing of pathogens. One effector arm of this network is the terminal pathway of complement, which leads to the formation of the membrane attack complex (MAC) composed of complement components C5b, C6, C7, C8 and C9. Upon formation of C5 convertases via the classical or alternative pathways of complement activation, C5b is generated from C5 by proteolytic cleavage, nucleating a series of association and polymerisation reactions of the MAC-constituting complement components that culminate in pore formation of pathogenic membranes. Recent structures of MAC components and homologous proteins significantly increased our understanding of oligomerisation, membrane association and integration, shedding light onto the molecular mechanism of this important branch of the innate immune system.

摘要

补体系统是血清蛋白的一个复杂网络,通过一个放大级联反应介导体液固有免疫,最终导致炎症细胞的募集、病原体的调理作用或杀伤。该网络的一个效应分支是补体的末端途径,它导致由补体成分C5b、C6、C7、C8和C9组成的膜攻击复合物(MAC)的形成。通过补体激活的经典或替代途径形成C5转化酶后,C5b通过蛋白水解切割从C5产生,引发构成MAC的补体成分的一系列缔合和聚合反应,最终导致致病膜形成孔道。MAC成分和同源蛋白的最新结构显著增进了我们对寡聚化、膜缔合和整合的理解,为这一固有免疫系统重要分支的分子机制提供了线索。

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