Factor H family proteins: on complement, microbes and human diseases

Author:

Zipfel P. F.1,Skerka C.1,Hellwage J.1,Jokiranta S. T.2,Meri S.2,Brade V.3,Kraiczy P.3,Noris M.4,Remuzzi G.4

Affiliation:

1. Hans Knoell Institute for Natural Products Research, Beutenbergstrasse I la, D-07745 Jena, Germany

2. Department of Bacteriology and Immunology, Haartman Institute, Haartmaninkatu 3, University of Helsinki, FIN-00290 Helsinki, Finland

3. Institute of Medical Microbiology, Frankfurt University Hospital, Paul-Ehrlich-Str. 40, D-60596 Frankfurt, Germany

4. Mario Negri Institute for Pharmacological Research, Bergamo, Italy

Abstract

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.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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