Structure and Function of the Trypanosome Flagellar Membrane

描述（由申请人提供）：锥虫鞭毛膜的结构和功能在原生动物寄生虫克氏锥虫和布氏锥虫的鞭毛中发现了许多密切相关的钙结合蛋白：cruzi和布氏锥虫的24 kDa（Tb-24）、25 kDa（Tb-17）和44 kDa（Tb-44）小牛精蛋白家族。这些蛋白质通过在其氨基末端添加肉豆蔻酸酯和棕榈酸酯来修饰，其介导鞭毛膜的定位。在上一个资助期内，已经确定了calflagins的各种性质：（i）它们与钙结合并经历钙诱导的构象变化，（ii）它们在鞭毛膜上的定位依赖于膜甾醇的浓度，（iii）它们似乎通过钙依赖性结合和推测的伴侣蛋白的调节发挥作用，（iv）它们具有与钙调蛋白相似但不同的独特三维结构，和（v）它们是鞭毛内运输（IFT）装置的组分和/或底物。此外，从这项工作中产生的相关发现包括以下内容：（i）鞭毛膜在化学上不同于薄膜膜，并显示出高度的液体秩序和脂质筏的富集，（ii）鞭毛DnaJ（hsp 40）蛋白参与胞质口的生物发生和（iii）鞘脂合成是T.布鲁塞。我们对FCaBP和calflagins的研究已经开始阐明这些蛋白在鞭毛功能和生物发生中的功能，并揭示了鞭毛膜作为招募双酰化蛋白和参与IFT的新平台。来自同事的信息表明，这些基本性质可能是共同的所有纤毛结构（鞭毛和感觉纤毛），因此锥虫可能是一个强大的模型系统，用于确定纤毛功能一般。我们计划在今后五年内对这些蛋白质进行深入的研究，并对鞭毛膜进行全面的研究，具体目标如下：（1）确定鞭毛蛋白靶向的分子决定因素。(2)研究鞭毛内运输和鞭毛膜运输之间的相互作用。(3)确定鞭毛膜的脂质组成及其对蛋白质靶向的贡献。

DESCRIPTION (provided by applicant): Structure and Function of the Trypanosome Flagellar Membrane A number of closely related calcium-binding proteins are found in the flagella of the protozoan parasites Trypanosoma cruzi and Trypanosoma brucei: a 24 kDa flagellar calcium binding protein (FCaBP) of T. cruzi and a family of 24 kDa (Tb-24), 25 kDa (Tb-17), and 44 kDa (Tb-44) calfagin proteins of Trypanosoma brucei. These proteins are modified by the addition of myristate and palmitate at their amino termini, which mediate localization to the flagellar membrane. Various properties of the calflagins have been determined during the previous funding period: (i) they bind calcium and undergo calcium-induced changes in conformation, (ii) their localization to the flagellar membrane is dependent on the concentration of membrane sterols, (iii) they appear to function through the calcium-dependent binding and presumed regulation of partner proteins, (iv) they have unique three-dimensional structures that are similar to but distinct from calmodulin and (v) they are components of and/or substrates for the intraflagellar transport (IFT) apparatus. Additional, related discoveries arising from from this work include the following: (i) the flagellar membrane is chemically distinct from the pellicular membrane and shows a high degree of liquid order and enrichment in lipid rafts, (ii) a flagellar DnaJ (hsp40) protein is involved in the biogenesis of the cytostome and (iii) sphingolipid synthesis is essential for normal cytokinesis and organelle segregation in T. brucei. Our work on FCaBP and the calflagins has begun to illuminate the functions of these proteins in flagellar function and biogenesis and has revealed the flagellar membrane as a novel platform for the recruitment of dually acylated proteins and participation in IFT. Information from colleagues indicate that these basic properties may be common to all ciliary structures (flagella and sensory cilia) and thus the trypanosome may be a powerful model system for the determination of ciliary function generally. We propose to extend our studies of these proteins specifically and the flagellar membrane generally in a five-year research effort having the following Specific Aims: (1) To define the molecular determinants of flagellar protein targeting. (2) To examine the interaction between intraflagellar transport and flagellar membrane trafficking. (3) To determine the lipid composition of the flagellar membrane and its contribution to protein targeting.