Crystal structure of a heparin- and integrin-binding segment of human fibronectin

被引:179
作者
Sharma, A
Askari, JA
Humphries, MJ
Jones, EY
Stuart, DI
机构
[1] Univ Oxford, Mol Biophys Lab, Oxford OX1 3QU, England
[2] Univ Manchester, Sch Biol Sci, Wellcome Trust Ctr Cell Matrix Res, Manchester M13 9PT, Lancs, England
[3] Oxford Ctr Mol Sci, New Chem Lab, Oxford OX1 3QT, England
基金
英国惠康基金;
关键词
fibronectin; heparin binding; integrin binding; protein structure; type III;
D O I
10.1093/emboj/18.6.1468
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
The crystal structure of human fibronectin (FN) type III repeats 12-14 reveals the primary heparin-binding site, a clump of positively charged residues in FN13, and a putative minor site similar to 60 Angstrom away in FN14. The IDAPS motif implicated in integrin alpha(4)beta(1) binding is at the FN13-14 junction, rendering the critical Asp184 inaccessible to integrin. Asp184 clamps the BC loop of FN14, whose sequence (PRARI) is reminiscent of the synergy sequence (PHSRN) of FN9. Mutagenesis studies prompted by this observation reveal that both arginines of the PRARI sequence are important for alpha(4)beta(1) binding to FN12-14. The PRARI motif may represent a new class of integrin-binding sites, The spatial organization of the binding sites suggests that heparin and integrin may bind in concert.
引用
收藏
页码:1468 / 1479
页数:12
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