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中文摘要
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描述(申请人提供):真菌细胞的细胞外基质称为细胞壁。细胞壁由互锁的蛋白质和多糖组成,在细胞和环境之间起到缓冲作用。在病原真菌中,细胞壁是寄主生存的关键。因此,参与细胞壁调节和组装的酶是抗真菌药物的极佳靶标。酿酒酵母的孢子壁是一种复杂的结构,在孢子形成过程中从头形成。孢子壁的组装为研究真菌壁组装过程和协调该过程的信号通路提供了一个很好的系统。Gip1-Glc7磷酸酶复合体介导了一条信号通路,只有在细胞质分裂完成后才能启动细胞壁的组装。对Gip1蛋白的结构-功能分析将被用来探索膜关闭触发Gip1-Glc7信号的基础。Gip1-Glc7调节途径下游成分转录因子Gis1的机制也将被阐明。尽管真菌细胞壁的成分已知,但将这些材料组装成功能壁的酶却鲜为人知。我们已经鉴定了几个编码与孢子壁形成有关的候选酶的基因。这些基因中突变的表型将被详细描述。此外,这些蛋白质的酶活性将使用体外组装试验进行检测。酿酒酵母的孢子壁成分也存在于病原体白色念珠菌的细胞壁中,它们对生物体的毒力很重要。我们将检查这些成分是否以与酿酒酵母孢子壁相似的方式组装到白色念珠菌的细胞壁中。孢子壁保护孢子免受一系列环境侵害的显著能力主要是由于孢子壁的外层。这些层有两个主要成分,壳聚糖,一种氨基葡萄糖多糖,和一种独特的含有交联型氨基酸二硫代赖氨酸的聚合物。这种双赖氨酸聚合物位于孢子壁的最外表面,部分起到扩散屏障的作用,限制了可溶性分子进出孢子壁的运动。为了更好地了解这种聚合物的功能,将结合使用质谱学和固态13C核磁共振来确定Dityroine聚合物的结构。 与公共卫生相关:真菌细胞壁是真菌细胞与环境之间的屏障。细胞壁对于真菌逃避宿主免疫反应是必不可少的,抗真菌药物通常通过干扰细胞壁的合成而起作用。本研究以酿酒酵母的孢子壁组装为研究对象,建立了霉菌壁组装的模型。实验的目标是了解壁组件的调节、组装路径和结构。
英文摘要
DESCRIPTION (provided by applicant): The extracellular matrix of fungal cells is referred to as the cell wall. The cell wall is composed of interlocked proteins and polysaccharides and serves as a buffer between the cell and its environment. In pathogenic fungi, the wall is critical for survival in the host. Enzymes involved in the regulation and assembly of the cell wall are therefore excellent targets for antifungal drugs. The spore wall of Saccharomyces cerevisiae is a complex structure that forms de novo during the process of sporulation. Assembly of the spore wall provides an excellent system to investigate both the process of fungal wall assembly and the signaling pathways that coordinate that process. The Gip1-Glc7 phosphatase complex mediates a signaling pathway that initiates assembly of the wall only after the completion of cytokinesis. A structure-function analysis of the Gip1 protein will be used to explore the basis by which membrane closure triggers Gip1-Glc7 signaling. The mechanism by which Gip1-Glc7 regulate a downstream component in the pathway, the transcription factor Gis1, will also be elucidated. Though the constituents of the fungal cell wall are known, the enzymes that assemble these materials into a functional wall are little understood. We have identified several genes encoding candidate enzymes involved in construction of the spore wall. These phenotypes of mutants in these genes will be characterized in detail. Additionally, the enzymatic activities of these proteins will be examined using an in vitro assembly assay. Components of the spore wall in S. cerevisiae are also found in the cell wall of the pathogen C. albicans where they are important for virulence of the organism. We will examine if these components are assembled into the C. albicans cell wall a similar fashion as in the S. cerevisiae spore wall. The remarkable ability of the spore wall to protect the spore from an array of environmental insults is due primarily to the outer layers of spore wall. These layers have two major constituents, chitosan, a glucosamine polysaccharide, and a unique polymer containing the crosslinked amino acid dityrosine. This dityrosine polymer is found on the outermost surface of the spore wall and acts in part as a diffusion barrier that limits the movement of soluble molecules into and out of the wall. To better understand how this polymer functions the structure of the dityrosine polymer will be determined using a combination of mass spectrometry and solid state 13C NMR. PUBLIC HEALTH RELEVANCE: Fungal cell walls act as a barrier between the fungal cell and its environment. The wall is essential for a fungal pathogen to evade the host immune response and antifungal drugs commonly act by interfering with wall synthesis. This study focuses on the assembly of the spore wall of baker's yeast, Saccharomyces cerevisiae, as a model for fungal wall assembly. Experiments are targeted towards understanding the regulation, assembly pathways, and structure of wall components.
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Mechanisms of de novo membrane assembly
INTERACTIONS BETWEEN PROTEINS OF THE MEIOTIC SPINDLE POLE BODY
  • 批准号:
    8365796
  • 项目类别:
  • 资助金额:
    $2.88万
  • 财政年份:
    2011
  • 负责人:
    Aaron M Neiman
  • 依托单位:
Chromatin and the Control of Late Meiotic Gene Expression
TRAINING IN LIVE CELL FLUORESCENCE MICROSCOPY AND FRET ANALYSIS
  • 批准号:
    7957817
  • 项目类别:
  • 资助金额:
    $0.68万
  • 财政年份:
    2009
  • 负责人:
    Aaron M Neiman
  • 依托单位:
海外基金