Downing A K, Knott V, Werner J M, Cardy C M, Campbell I D, Handford P A
Department of Biochemistry University of Oxford, United Kingdom.
Cell. 1996 May 17;85(4):597-605. doi: 10.1016/s0092-8674(00)81259-3.
The nuclear magnetic resonance structure of a covalently linked pair of calcium-binding (cb) epidermal growth factor-like (EGF) domains from human fibrillin-1, the protein defective in the Marfan syndrome, is described. The two domains are in a rigid, rod-like arrangement, stabilized by interdomain calcium binding and hydrophobic interactions. We propose a model for the arrangement of fibrillin monomers in microfibrils that reconciles structural and antibody binding data, and we describe a set of disease-causing mutations that provide the first clues to the specificity of cbEFG interactions. The residues involved in stabilizing the domain linkage are highly conserved in fibrillin, fibulin, thrombomodulin, and the low density lipoprotein receptor. We propose that the relative orientation of tandem cbEGF domains in these proteins is similar, but that in others, including Notch, pairs adopt a completely different conformation.
本文描述了来自人原纤蛋白-1的一对共价连接的钙结合(cb)表皮生长因子样(EGF)结构域的核磁共振结构,原纤蛋白-1是马凡氏综合征中出现缺陷的蛋白质。这两个结构域呈刚性的棒状排列,通过结构域间的钙结合和疏水相互作用得以稳定。我们提出了一个原纤蛋白单体在微原纤维中排列的模型,该模型整合了结构和抗体结合数据,并且我们描述了一组致病突变,这些突变首次为cbEFG相互作用的特异性提供了线索。在原纤蛋白、纤连蛋白、血栓调节蛋白和低密度脂蛋白受体中,参与稳定结构域连接的残基高度保守。我们认为,这些蛋白质中串联cbEGF结构域的相对取向相似,但在其他蛋白质中,包括Notch,其结构域对则采用完全不同的构象。