Tonkin Michelle L, Beck Josh R, Bradley Peter J, Boulanger Martin J
From the Department of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia V8W 3P6, Canada and.
Department of Microbiology, Immunology, and Molecular Genetics, UCLA, Los Angeles, California 90095.
J Biol Chem. 2014 May 16;289(20):13962-73. doi: 10.1074/jbc.M114.548891. Epub 2014 Mar 27.
Toxoplasma gondii, an apicomplexan parasite prevalent in developed nations, infects up to one-third of the human population. The success of this parasite depends on several unique structures including an inner membrane complex (IMC) that lines the interior of the plasma membrane and contains proteins important for gliding motility and replication. Of these proteins, the IMC sub-compartment proteins (ISPs) have recently been shown to play a role in asexual T. gondii daughter cell formation, yet the mechanism is unknown. Complicating mechanistic characterization of the ISPs is a lack of sequence identity with proteins of known structure or function. In support of elucidating the function of ISPs, we first determined the crystal structures of representative members TgISP1 and TgISP3 to a resolution of 2.10 and 2.32 Å, respectively. Structural analysis revealed that both ISPs adopt a pleckstrin homology fold often associated with phospholipid binding or protein-protein interactions. Substitution of basic for hydrophobic residues in the region that overlays with phospholipid binding in related pleckstrin homology domains, however, suggests that ISPs do not retain phospholipid binding activity. Consistent with this observation, biochemical assays revealed no phospholipid binding activity. Interestingly, mapping of conserved surface residues combined with crystal packing analysis indicates that TgISPs have functionally repurposed the phospholipid-binding site likely to coordinate protein partners. Recruitment of larger protein complexes may also be aided through avidity-enhanced interactions resulting from multimerization of the ISPs. Overall, we propose a model where TgISPs recruit protein partners to the IMC to ensure correct progression of daughter cell formation.
刚地弓形虫是一种在发达国家普遍存在的顶复门寄生虫,感染着多达三分之一的人类。这种寄生虫的成功寄生依赖于几种独特的结构,包括内膜复合体(IMC),它位于质膜内部,含有对滑行运动和复制至关重要的蛋白质。在这些蛋白质中,IMC亚区室蛋白(ISPs)最近被证明在刚地弓形虫无性繁殖的子细胞形成中发挥作用,但其机制尚不清楚。由于与已知结构或功能的蛋白质缺乏序列同一性,使得对ISPs进行机制表征变得复杂。为了支持阐明ISPs的功能,我们首先确定了代表性成员TgISP1和TgISP3的晶体结构,分辨率分别为2.10 Å和2.32 Å。结构分析表明,这两种ISPs都采用了通常与磷脂结合或蛋白质-蛋白质相互作用相关的普列克底物蛋白同源结构域。然而,在与相关普列克底物蛋白同源结构域中与磷脂结合重叠的区域,用碱性残基取代疏水残基表明ISPs不保留磷脂结合活性。与此观察结果一致,生化分析显示没有磷脂结合活性。有趣的是,保守表面残基的图谱分析与晶体堆积分析相结合表明,TgISPs已经在功能上重新利用了可能用于协调蛋白质伙伴的磷脂结合位点。ISPs的多聚化导致的亲和力增强相互作用也可能有助于募集更大的蛋白质复合物。总体而言,我们提出了一个模型,其中TgISPs将蛋白质伙伴募集到IMC,以确保子细胞形成的正确进程。