Askari Janet A, Thornton David J, Humphries Jonathan D, Buckley Patrick A, Humphries Martin J
Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Matrix Biol. 2007 Jul;26(6):485-93. doi: 10.1016/j.matbio.2007.04.001. Epub 2007 Apr 6.
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 12-15, and including the alternatively-spliced type three connecting segment (IIICS), was found to bind Ni(2+), Cu(2+) and Zn(2+) 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.
纤连蛋白(FN)是一种典型的黏附糖蛋白,广泛存在于细胞外基质和体液中。纤连蛋白分子是二聚体,由一系列重复的多肽模块组成。研究发现,包含III型重复序列12 - 15并含有选择性剪接的III型连接段(IIICS)的FN重组片段能够结合Ni(2+)、Cu(2+)和Zn(2+)二价阳离子,而缺乏IIICS的类似片段则不能。在IIICS不同剪接区域的两对组氨酸残基发生突变,使阳离子结合能力降低至接近缺乏IIICS的变体水平,这表明存在类似锌指的阳离子配位模式。对从血浆或羊水中纯化的天然FN进行分析发现,与那些含有完整IIICS的同种型相关的锌含量显著。综上所述,这些数据表明FN的IIICS区域是一个新的锌结合模块。