Integrin αvβ3 binds a unique non-RGD site near the C-terminus of human tropoelastin

被引:92
作者
Rodgers, UR [1 ]
Weiss, AS [1 ]
机构
[1] Univ Sydney, Sch Mol & Microbial Biosci, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会;
关键词
elastin; extracellular matrix; integrins; tropoelastin;
D O I
10.1016/j.biochi.2004.03.002
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
Tropoelastin is the soluble precursor of the essential resilient connective tissue protein elastin. We examined the binding of integrin alpha(v)beta(3) to tropoelastin. In quantitative colorimetric solid-phase assays, purified alpha(v)beta(3) demonstrated saturable, divalent cation-dependent, single-site binding behavior on tropoelastin with a dissociation constant of 3.8 +/- 0.9 nM in the presence of 1 mM Mn2+ which increased to 23 5 nM in the presence of 1 mM Ca2+ . Association with alpha(v)beta(3) was localized to the C-terminal 16 residues of tropoelastin, encompassing the region encoded by exon 36. This region comprises a unique disulfide loop in tropoelastin that is not essential for the interaction. This is the first identification of a specific, single binding site on tropoelastin and the first observation of direct binding of an integrin to a tropoelastin domain. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:173 / 178
页数:6
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