Zipfel P F, Skerka C, Hellwage J, Jokiranta S T, Meri S, Brade V, Kraiczy P, Noris M, Remuzzi G
Hans Knoell Institute for Natural Products Research, Beutenbergstrasse 11a, D-07745 Jena, Germany.
Biochem Soc Trans. 2002 Nov;30(Pt 6):971-8. doi: 10.1042/bst0300971.
At present, the human Factor H protein family represents seven multidomain, multifunctional serum proteins. This group includes the complement and immune regulators Factor H, the Factor H-like protein 1 (FHL-1) and five Factor H-related proteins proteins (FHR-1, -2, -3, -4 and -5). Each is exclusively composed of individually folded protein domains, termed short consensus repeats (SCRs) or complement control modules. Structure-function analyses allowed the localization of the complement regulatory domain of Factor H and FHL-1 in the N-terminal region within SCRs 1-4. In addition, multiple binding sites for C3b, heparin and microbial surface proteins were localized in the N-terminus, within the middle region and also in the C-terminus of Factor H and FHL-1. Recent results show a central role for the C-terminus of Factor H, i.e. SCRs 19-20. These particular domains are conserved in all FHRs identified so far, include contact points for C3b, heparin and microbial surface proteins and represent a 'hot-spot' for gene mutations in patients that suffer from the Factor H-associated form of haemolytic uraemic syndrome.
目前,人源补体因子H蛋白家族由七种多结构域、多功能血清蛋白组成。该家族包括补体和免疫调节因子补体因子H、补体因子H样蛋白1(FHL-1)以及五种补体因子H相关蛋白(FHR-1、-2、-3、-4和-5)。它们均仅由单独折叠的蛋白结构域组成,这些结构域被称为短共识重复序列(SCR)或补体控制模块。结构-功能分析确定了补体因子H和FHL-1的补体调节结构域位于SCR 1-4的N端区域。此外,补体因子H和FHL-1的N端、中间区域以及C端均存在多个与C3b、肝素和微生物表面蛋白结合的位点。最近的研究结果表明补体因子H的C端(即SCR 19-20)起着核心作用。这些特定结构域在迄今鉴定出的所有FHR中均保守,包含与C3b、肝素和微生物表面蛋白的结合位点,并且是患有补体因子H相关型溶血尿毒综合征患者基因突变的“热点”。