Structural basis for host recognition by the Haemophilus influenzae Hia autotransporter

被引:77
作者
Yeo, HJ
Cotter, SE
Laarmann, S
Juehne, T
St Geme, JW
Waksman, G
机构
[1] Univ London Birkbeck Coll, Sch Crystallog, Inst Struct Mol Biol, London WC1E 7HX, England
[2] UCL, Dept Biochem & Mol Biol, London, England
[3] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Edward Mallinckrodt Dept Pediat, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
基金
英国惠康基金;
关键词
adhesion; autotransporter; crystal structure; homotrimer; microbial pathogenesis;
D O I
10.1038/sj.emboj.7600142
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Haemophilus influenzae is an important human pathogen that initiates infection by colonizing the upper respiratory tract. The H. influenzae Hia autotransporter is an adhesive protein that promotes adherence to respiratory epithelial cells. Hia adhesive activity resides in two homologous binding domains, called HiaBD1 and HiaBD2. These domains interact with the same host cell receptor, but bind with different affinities. In this report, we describe the crystal structure of the high-affinity HiaBD1 binding domain, which has a novel trimeric architecture with three-fold symmetry and a mushroom shape. The subunit constituents of the trimer are extensively intertwined. The receptor-binding pocket is formed by an acidic patch that is present on all three faces of the trimer, providing potential for a multivalent interaction with the host cell surface, analogous to observations with the trimeric tumor necrosis factor superfamily of proteins. Hia is a novel example of a bacterial trimeric adhesin and may be the prototype member of a large family of bacterial virulence proteins with a similar architecture.
引用
收藏
页码:1245 / 1256
页数:12
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