Oppermann M, Manuelian T, Józsi M, Brandt E, Jokiranta T S, Heinen S, Meri S, Skerka C, Götze O, Zipfel P F
Department of Immunology, University of Göttingen, Göttingen, Germany.
Clin Exp Immunol. 2006 May;144(2):342-52. doi: 10.1111/j.1365-2249.2006.03071.x.
The complement inhibitor Factor H has three distinct binding sites for C3b and for heparin, but in solution uses specifically the most C-terminal domain, i.e. short consensus repeats (SCR) 20 for ligand interaction. Two novel monoclonal antibodies (mABs C14 and C18) that bind to the most C-terminal domain SCR 20 completely blocked interaction of Factor H with the ligands C3b, C3d, heparin and binding to endothelial cells. In contrast, several mAbs that bind to the N-terminus and to the middle regions of the molecule showed no or minor inhibitory effects when assayed by enzyme-linked immunosorbent assay (ELISA) and ligand interaction assays. This paradox between a single functional binding site identified for native Factor H versus multiple interaction sites reported for deletion constructs is explained by a compact conformation of the fluid phase protein with one accessible binding site. On zymosan particles mAbs C14 and C18 blocked alternative pathway activation completely. Thus demonstrating that native Factor H makes the first and initial contact with the C terminus, which is followed by N terminally mediated complement regulation. These results are explained by a conformational hypothetical model: the native Factor H protein has a compact structure and only one binding site accessible. Upon the first contact the protein unfolds and exposes the additional binding sites. This model does explain how Factor H mediates recognition functions during complement control and the clustering of disease associated mutations in patients with haemolytic uraemic syndrome that have been reported in the C-terminal recognition domain of Factor H.
补体抑制剂H因子对C3b和肝素具有三个不同的结合位点,但在溶液中特异性地使用最末端结构域,即用于配体相互作用的短共有重复序列(SCR)20。两种与最末端结构域SCR 20结合的新型单克隆抗体(mABs C14和C18)完全阻断了H因子与配体C3b、C3d、肝素的相互作用以及与内皮细胞的结合。相比之下,通过酶联免疫吸附测定(ELISA)和配体相互作用测定分析时,几种与分子N末端和中间区域结合的单克隆抗体没有显示或仅有轻微的抑制作用。天然H因子确定的单个功能结合位点与缺失构建体报道的多个相互作用位点之间的这种矛盾,可通过具有一个可及结合位点的液相蛋白的紧密构象来解释。在酵母聚糖颗粒上,mABs C14和C18完全阻断了替代途径的激活。因此证明天然H因子首先与C末端进行初始接触,随后是由N末端介导的补体调节。这些结果可用一个构象假设模型来解释:天然H因子蛋白具有紧密结构,只有一个可及结合位点。首次接触后,该蛋白展开并暴露出其他结合位点。该模型确实解释了H因子在补体控制过程中如何介导识别功能,以及在溶血尿毒综合征患者中H因子C末端识别域所报道的与疾病相关突变的聚集情况。