Functional Studies of Ubiquilin
Functional Studies of Ubiquilin
批准号:
6891074
负责人:
Mervyn J Monteiro
金额:
$29.4万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-05-01 至 2007-04-30
关键词:
Caenorhabditis elegansantibody neutralization testcell free systemgreen fluorescent proteinshuman tissueimmunoprecipitationlaboratory mouselaboratory ratmolecular cloningnorthern blottingsnuclear proteinsnucleic acid sequencepolymerase chain reactionproteasomeprotein degradationprotein isoformsprotein localizationprotein structure functionsite directed mutagenesistissue /cell culturetransfectionubiquitinwestern blottingsyeast two hybrid system
中文摘要
描述(由申请人提供):神经退行性疾病研究中出现的一个共同主题是泛素-蛋白酶体系统中错误折叠的蛋白质和缺陷的参与。泛素-蛋白酶体系统最初被认为是标记和销毁不需要的蛋白质的机制。然而,最近的证据表明,泛素-蛋白酶体系统也参与了蛋白质的去折叠、细胞内的蛋白质靶向、细胞信号和转录。我们的实验室发现了泛素,它是一类令人兴奋的新蛋白质的创始成员,似乎可以抑制蛋白质的降解。泛素含有多种泛素相关基序,通常存在于泛素-蛋白酶体系统中的蛋白质中。我们通过泛素与早老素蛋白的相互作用来鉴定泛素,这种蛋白的突变与早发性家族性阿尔茨海默病有关。泛素在细胞中的过表达增加了早老素蛋白的水平,降低了内蛋白水解性N端和C端早老素片段的水平,并减少了早老素蛋白的泛素化。包括我们实验室的结果在内的几条证据表明,泛素在细胞应激过程中被诱导表达,它可能作为分子伴侣、泛素受体或在细胞生存中发挥作用。
我们建议使用多管齐下的方法来确定泛素蛋白在细胞和生物体中所起的作用。利用细胞、分子和免疫学技术,我们将确定不同泛素蛋白在组织和组织培养细胞中的表达模式以及不同泛素亚型的细胞内定位特性。我们将确定泛素多肽的不同结构域如何参与蛋白质的功能。我们将使用两种转染法以及体外无细胞翻译试验来确定泛素在泛素-蛋白酶体系统中所起的作用。我们将使用免疫共沉淀和酵母双杂交试验来鉴定泛素相互作用蛋白。最后,我们建议使用小鼠的基因敲除,线虫和人类组织培养细胞的反义抑制,以及抗体中和来鉴定泛素缺失对细胞和生物的影响。从拟议的研究中获得的结果将有助于更好地理解泛素在细胞和整个生物体中的功能作用,并最终了解其在健康和疾病中的作用。
英文摘要
DESCRIPTION (provided by applicant): A common theme that is emerging from studies of neurodegenerative disorders is the involvement of misfolded proteins and defects in the ubiquitin-proteasome system. The ubiquitin-proteasome system was originally considered to be the machinery for tagging and destroying unwanted proteins. However, recent evidence indicates that the ubiquitin-proteasome system is also involved in protein unfolding, intracellular protein targeting, cell signaling and transcription. Our laboratory identified ubiquilin, the founding member of an exciting new class of proteins, which appears to inhibit degradation of proteins. Ubiquilin contains multiple ubiquitin-related motifs typically found in proteins involved in the ubiquitin-proteasome system. We identified ubiquilin through its interactions with presenilin proteins, mutations in which are associated with early-onset familial Alzheimer's disease. Overexpression of ubiquilin in cells increases presenilin protein levels, decreases levels of endoproteolytic N- and C-terminal presenilin fragments, and decreases ubiquitination of presenilin proteins. Several lines of evidence, including results from our laboratory, suggest that ubiquilin expression is induced during cell stress and that it may function as a molecular chaperone, a ubiquitin-receptor, or in cell survival.
We propose to use a multi-pronged approach to determine the role ubiquilin proteins play in cells and organisms. Using cellular, molecular, and immunological techniques, we will determine the expression patterns of the different ubiquilin proteins in tissues and tissue culture cells as well as the intracellular localization properties of different ubiquilin isotypes. We will determine how different domains of the ubiquilin polypeptide are involved in the functions of the protein. We will use both transfection assays, as well as an in vitro cell-free translation assay, to identify the role ubiquilin plays in the ubiquitin-proteasome system. We will characterize ubiquilin-interacting proteins using co-immunoprecipitation and yeast two-hybrid assays. Finally, we propose to use gene knockout in mouse, anti-sense inhibition in C. elegans and human tissue culture cells, and antibody neutralization to identify the effects that loss of ubiquilin has in cells and organisms. The results obtained from the proposed research will lead to a better understanding of the functional role of ubiquilin in cells and in whole organisms, and ultimately, its role in health and in disease.
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会议论文
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