The alternatively spliced type III connecting segment of fibronectin is a zinc-binding module

被引:6
作者
Askari, Janet A. [1 ]
Thornton, David J. [1 ]
Humphries, Jonathan D. [1 ]
Buckley, Patrick A. [1 ]
Humphries, Martin J. [1 ]
机构
[1] Univ Manchester, Wellcome Trust Ctr Cell Matrix Res, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
fibronectin; zinc; IIICS region; cation-binding; alternative splicing;
D O I
10.1016/j.matbio.2007.04.001
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
Fibronectin (FN) is a prototypic adhesive glycoprotein that is widely expressed in extracellular matrices and body fluids. The fibronectin molecule is dimeric, and composed of a series of repeating polypeptide modules. A recombinant fragment of FN incorporating type III repeats 1215, and including the altematively-spliced type three connecting segment (IIICS), was found to bind Ni2+ Cu2+ and Zn2+ divalent cations, whereas a similar fragment lacking the IIICS did not. Mutation of two pairs of histidine residues in separate spliced regions of the IIICS reduced cation binding to near the level of the variant lacking the IIICS, suggesting a zinc finger-like mode of cation coordination. Analysis of native FNs purified from plasma or amniotic fluid revealed significant levels of zinc associated with those isoforms that contain the complete IIICS. Taken together, these data demonstrate that the IIICS region of FN is a novel zinc-binding module. (c) 2007 Elsevier B.V./International Society of Matrix Biology. All rights reserved.
引用
收藏
页码:485 / 493
页数:9
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