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补体调节因子H疾病相关T1184R变体的晶体学测定

Crystallographic determination of the disease-associated T1184R variant of complement regulator factor H.

作者信息

Morgan Hugh P, Jiang Jingzi, Herbert Andrew P, Kavanagh David, Uhrin Dušan, Barlow Paul N, Hannan Jonathan P

机构信息

Institute of Structural and Molecular Biology, School of Biological Sciences, University of Edinburgh, King's Buildings, Mayfield Road, Scotland.

出版信息

Acta Crystallogr D Biol Crystallogr. 2011 Jul;67(Pt 7):593-600. doi: 10.1107/S0907444911015423. Epub 2011 Jun 11.

Abstract

The soluble 155 kDa glycoprotein factor H (FH) protects host tissue from damage by the human complement system. It accelerates decay of the alternative-pathway C3 convertase, C3bBb, and is a cofactor for factor I-mediated cleavage of the opsonin C3b. Numerous mutations and single-nucleotide polymorphisms (SNPs) occur in the gene encoding FH and the resulting missense mutations and truncation products result in altered functionality that predisposes to the development of the serious renal condition atypical haemolytic uraemic syndrome (aHUS). Other polymorphisms are linked to membranoproliferative glomerulonephritis and macular degeneration. The two C-terminal modules of FH (FH19-20) harbour numerous aHUS-associated mutations that disrupt the ability of factor H to protect host cells from complement-mediated damage. In this work, the crystal structure of an aHUS-associated T1184R variant of FH19-20 at a resolution of 1.52 Å is described. It is shown that this mutation has negligible structural effects but causes a significant change in the electrostatic surface of these two domains. Mechanisms are discussed by which this mutation may alter FH-ligand interactions, particularly with regard to the extension of a region of this molecule within module 20 that has been associated with the binding of glycosaminoglycans (GAGs) or sialic acid residues.

摘要

可溶性155 kDa糖蛋白H因子(FH)可保护宿主组织免受人类补体系统的损伤。它能加速替代途径C3转化酶C3bBb的衰变,并且是I因子介导的调理素C3b裂解的辅因子。编码FH的基因中存在大量突变和单核苷酸多态性(SNP),由此产生的错义突变和截短产物会导致功能改变,进而易引发严重的肾脏疾病——非典型溶血性尿毒症综合征(aHUS)。其他多态性与膜增生性肾小球肾炎和黄斑变性有关。FH的两个C末端模块(FH19 - 20)含有许多与aHUS相关的突变,这些突变破坏了H因子保护宿主细胞免受补体介导损伤的能力。在这项工作中,描述了FH19 - 20的aHUS相关T1184R变体的晶体结构,分辨率为1.52 Å。结果表明,该突变对结构的影响可忽略不计,但会导致这两个结构域的静电表面发生显著变化。文中讨论了这种突变可能改变FH - 配体相互作用的机制,特别是关于该分子在模块20内与糖胺聚糖(GAG)或唾液酸残基结合相关区域的延伸。

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