Mechanism and function of ubiquitin binding by conserved endocytic protein Rvs167
Mechanism and function of ubiquitin binding by conserved endocytic protein Rvs167
批准号:
8240621
负责人:
Margaret Myers
金额:
$2.74万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-15 至 2011-09-14
关键词:
ActinsAffinity ChromatographyAmino AcidsBindingBiological AssayCell physiologyCellsChimeric ProteinsClathrinDefectDown-RegulationEndocytosisEukaryotic CellFoundationsFungal GenomeGrowthHomologous ProteinHumanHybridsMammalsMediatingMembraneMicrofilamentsMicroscopyMolecularMonitorNutrientPhasePlayProcessProteinsReceptor SignalingRecombinantsRecyclingRelative (related person)RoleStructureSynaptic VesiclesTertiary Protein StructureTimeUbiquitinYeastsamphiphysinbasecell growthdeprivationhuman diseasemutantnovelresponseuptake
中文摘要
描述(申请人提供):网状蛋白介导的内吞作用是一个在所有真核细胞中都保守的基本过程,是许多重要功能所必需的,包括营养吸收、膜重塑、突触小泡循环和激活的信号受体的下调。Rvs167是一种杆状结构域蛋白,与哺乳动物的内吞因子内嗜素和两栖菌素同源,是酵母生长控制和内吞作用所必需的。最近,Rvs167被证明与泛素结合,初步研究表明,Rvs167的功能需要泛素结合。本申请提出通过以下目的来确定Rvs167与泛素结合的机制和功能:1)通过与重组Rvs167的不同片段或突变体进行结合分析,确定Rvs167与泛素之间新的相互作用的分子基础。2)确定泛素结合在细胞生长、肌动蛋白组织和内吞作用中的作用。将分析泛素结合缺陷细胞的生长停滞,以响应营养剥夺、肌动蛋白细丝结构以及体相和受体依赖标记物的内吞。此外,实时荧光显微镜将用于监测Rvs167野生型和泛素结合缺陷荧光蛋白在共表达其他具有替代荧光标签的内吞蛋白的菌株中的定位和动态。3)鉴定与Rvs167通过泛素结合相互作用的蛋白(S)。相互作用的蛋白质将通过全基因组酵母-2-杂交筛选、GST融合蛋白亲和层析或从酵母裂解物中免疫共沉淀来鉴定。一旦确定,相互作用蛋白的缺失和Rvs167结合缺陷突变体将接受目标2中描述的分析。这些研究有望有助于理解内吞作用和细胞生长控制的分子机制,并为了解内吞作用缺陷如何导致人类疾病提供基础。内吞作用是一种基本的细胞过程,从酵母到人类都是保守的。Rvs167是两种人类内吞蛋白的近亲,是酵母生长控制和内吞作用所必需的。这些关于Rvs167的研究有望有助于理解引起内吞作用的基本分子机制,并为理解内吞作用缺陷如何导致人类疾病提供基础。
英文摘要
DESCRIPTION (provided by applicant): Clathrin-mediated endocytosis is a fundamental process that is conserved in all eukaryotic cells, and is required for numerous important functions including nutrient uptake, membrane remodeling, synaptic vesicle recycling and down-regulation of activated signaling receptors. Rvs167, a BAR domain protein homologous to the mammalian endocytic factors endophilin and amphiphysin, is required for growth control and endocytosis in yeast. Recently, Rvs167 was demonstrated to bind ubiquitin, and preliminary studies suggest that ubiquitin binding is required for the function of Rvs167. This application proposes to define the mechanism and function of ubiquitin binding by Rvs167 through the following aims: 1) Determine the molecular basis for the novel interaction between Rvs167 and ubiquitin by conducting binding assays with different fragments or mutants of recombinant Rvs167. 2) Define the role of ubiquitin binding in cell growth, actin organization and endocytosis. Ubiquitin binding-defective cells will be analyzed for growth arrest in response to nutrient deprivation, actin filament structure, and endocytosis of both bulk-phase and receptordependent markers. Additionally, real-time fluorescent microscopy will be used to monitor the localization and dynamics of wild-type and ubiquitin binding-defective fluorescent protein fusions of Rvs167 in strains co-expressing other endocytic proteins with alternate fluorescent tags. 3) Identify and characterize protein(s) that interact with Rvs167 via ubiquitin binding. Interacting proteins will be identified by a whole genome yeast-2-hybrid screen, GST fusion protein affinity chromatography, or by coimmunoprecipitation from yeast lysates. Once identified, deletion and Rvs167-binding defective mutants of interacting proteins will be subjected to assays described in aim 2. These studies are anticipated to contribute to understanding of the molecular mechanisms responsible for endocytosis and cell growth control, and to provide a foundation to understand how defects in endocytosis contribute to human disease. Endocytosis is a fundamental cellular process that is conserved from yeast to humans. Rvs167 is a close relative of two human endocytic proteins and is required for growth control and endocytosis in yeast. These studies on Rvs167 are anticipated to contribute to understanding the basic molecular mechanisms responsible for endocytosis and to provide a foundation for understanding how defects in endocytosis contribute to human disease.
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Mechanism and function of ubiquitin binding by conserved endocytic protein Rvs167
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批准号:7540534
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项目类别:
-
资助金额:$4.96万
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财政年份:2008
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负责人:Margaret Myers
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依托单位:
Mechanism and function of ubiquitin binding by conserved endocytic protein Rvs167
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批准号:7683958
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项目类别:
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资助金额:$5.17万
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财政年份:2008
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负责人:Margaret Myers
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依托单位:
Mechanism and function of ubiquitin binding by conserved endocytic protein Rvs167
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批准号:7912905
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项目类别:
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资助金额:$2.69万
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财政年份:2008
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负责人:Margaret Myers
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依托单位:
海外基金