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Structural analysis of the plakin domain of bullous pemphigoid antigen1 (BPAG1) suggests that plakins are members of the spectrin superfamily

机译:大疱性类天疱疮抗原1(BPAG1)的plakin域的结构分析表明,plakins是血影蛋白超家族的成员

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摘要

Bullous pemphigoid antigen 1 (BPAG1) is a member of the plakin family of proteins. The plakins are multi-domain proteins that have been shown to interact with microtubules, actin filaments and intermediate filaments, as well as proteins found in cellular junctions. These interactions are mediated through different domains on the plakins. The interactions between plakins and components of specialized cell junctions such as desmosomes and hemidesmosomes are mediated through the so-called plakin domain, which is a common feature of the plakins. We report the crystal structure of a stable fragment from BPAG1, residues 226-448, defined by limited proteolysis of the whole plakin domain. The structure, determined by single-wavelength anomalous diffraction phasing from a selenomethionine-substituted crystal at 3.0 angstrom resolution, reveals a tandem pair of triple helical bundles closely related to spectrin repeats. Based on this structure and analysis of sequence conservation, we propose that the architecture of plakin domains is defined by two pairs of spectrin repeats interrupted by a putative Src-Homology 3 (SH3) domain. (c) 2006 Elsevier Ltd. All rights reserved.
机译:大疱性类天疱疮抗原1(BPAG1)是蛋白的plakin家族的成员。 plakins是已显示与微管,肌动蛋白丝和中间丝以及在细胞接头中发现的蛋白相互作用的多域蛋白。这些相互作用是通过普通蛋白的不同结构域介导的。 plakin与专门的细胞连接的组分如桥粒和半桥粒之间的相互作用是通过所谓的plakin结构域介导的,这是plakin的共同特征。我们报告了BPAG1,残基226-448,由有限的整个plakin域蛋白水解定义的稳定片段的晶体结构。该结构是由硒代蛋氨酸取代的晶体在3.0埃分辨率下通过单波长异常衍射确定的,揭示了一对串联的三螺旋束,它们与血影蛋白重复密切相关。基于这种结构和序列保守性的分析,我们建议通过两个假定的Src-Homology 3(SH3)域中断的两对血影蛋白重复序列​​来定义plakin域的体系结构。 (c)2006 Elsevier Ltd.保留所有权利。

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