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Quantifying post-translational modifications and protein expression by HTP-MS

Quantifying post-translational modifications and protein expression by HTP-MS
通过 HTP-MS 定量翻译后修饰和蛋白质表达
批准号:
8046203
负责人:
MARC Wallace KIRSCHNER
金额:
$377.85万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-30 至 2013-08-31

项目摘要

项目成果

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中文摘要
翻译
描述(申请人提供):本申请回应了应用基因组学和其他高通量技术的需求和机会。我们的目标是使用一种新开发的质谱学技术FLEXIQuant,提供几种不同细胞系中1,000种蛋白质水平的绝对定量。在提供定量的同时,FLEXIQuant还提供有关蛋白质中哪些多肽被修饰以及修饰程度的信息。这个项目的最终成果如下:(1)1,000个克隆在FLEXIQuant载体中,存放在一个非营利性的质粒库中,并免费提供给社区;(2)对于与这些克隆对应的蛋白质,一个全面的多肽数据库,在用4种不同的蛋白酶消化后,可在质谱学实验中检测到;(3)对于与这些克隆对应的mRNAs,一个全面的数据库,量化6个细胞系在不同条件下的mRNAs水平;以及(4)一个数据库,比较这些克隆在相同细胞系中,在相同条件下的mRNA水平、蛋白质水平和翻译后修饰。这项工作将首次开启基因组水平上的翻译后修饰研究,并将为社区分析提供一系列重要数据。这一数据集将允许的问题/方法类型包括:(1)监测我们数据集中任何蛋白质的水平和修饰;(2)测量不同细胞类型之间蛋白质水平和/或修饰的变异性;(3)将疾病状态或表型与蛋白质水平和修饰相关联;以及(4)通过比较mRNA和蛋白质水平来寻找翻译调控的来源。我们选择了一组蛋白质,包括参与和诱导WNT信号的基因,所有的激酶,所有的磷酸酶,以及参与细胞周期的基因;我们将测量这些基因在肝癌细胞系、结直肠癌细胞系和永生化的视网膜上皮系中的水平和修饰。我们提供的数据将成为许多致力于癌症细胞生物学的实验室的重要资源。 公共卫生相关性:我们提出了一个项目,准确地测量1000种蛋白质的水平,同时检测和量化六种不同细胞系中这些蛋白质的所有修饰。这些数据应该会大大增加我们对这些蛋白质的行为的理解,特别是在癌细胞中,开辟一种新的方法来理解生物系统是如何工作的,并为创建疾病的生物标记物提供一条新的途径。
英文摘要
DESCRIPTION (provided by applicant): This application responds to the needs and opportunities in Applying Genomics and Other High Throughput Technologies. We aim to use a newly-developed mass spectroscopy technique, FLEXIQuant, to provide absolute quantitation of the levels of 1,000 proteins in several different cell lines. At the same time as providing quantitation, FLEXIQuant provides information on which peptides in a protein are modified, and to what extent. Our ultimate deliverables from this project will be as follows: (1) A set of 1,000 clones in FLEXIQuant vectors, deposited with a non-profit plasmid repository and freely available to the community; (2) for the proteins corresponding to these clones, a comprehensive database of peptides detectable in mass spectroscopy experiments after digestion with 4 different proteases; (3) for the mRNAs corresponding to these clones, a comprehensive database quantitating the levels of mRNAs in 6 cell lines under different conditions; and (4) a database comparing mRNA levels, protein levels, and post- translational modifications for these clones in the same cell lines, under the same conditions. This work will for the first time open up the study of post-translational modifications on the genomic level, and will provide a range of important data for analysis by the community. Types of questions/approaches this dataset will allow include (1) monitoring the level of and modifications on any of the proteins in our dataset; (2) measuring the variability in protein level and/or modifications between different cell types; (3) correlating disease state or phenotypes with protein levels and modifications; and (4) finding sources of translational regulation by comparing mRNA and protein levels. We have chosen a set of proteins that includes genes involved in and induced by wnt signaling, all kinases, all phosphatases, and genes involved in the cell cycle; we will measure the levels and modifications of these in hepatocarcinoma cell lines, colorectal cancer lines, and an immortalized retinal epithelium line. The data we deliver will be an important resource for many labs working on the cell biology of cancer. PUBLIC HEALTH RELEVANCE: We propose a project to accurately measure the levels of 1,000 proteins, and at the same time detect and quantitate all the modifications on these proteins in six different cell lines. These data should provide a very significant increase in our understanding of the behavior of these proteins, especially in cancer cells, open up a new type of approach to understanding how biological systems work, and provide a novel route to the creation of biomarkers for disease.
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The dynamics and underlying mechanisms controlling cell size and canonical Wnt signaling
  • 批准号:
    10670148
  • 项目类别:
  • 资助金额:
    $74.92万
  • 财政年份:
    2022
  • 负责人:
    MARC Wallace KIRSCHNER
  • 依托单位:
The dynamics and underlying mechanisms controlling cell size and canonical Wnt signaling
  • 批准号:
    10797294
  • 项目类别:
  • 资助金额:
    $13.3万
  • 财政年份:
    2022
  • 负责人:
    MARC Wallace KIRSCHNER
  • 依托单位:
The dynamics and underlying mechanisms controlling cell size and canonical Wnt signaling
  • 批准号:
    10405995
  • 项目类别:
  • 资助金额:
    $74.92万
  • 财政年份:
    2022
  • 负责人:
    MARC Wallace KIRSCHNER
  • 依托单位:
Reverse Engineering of Cell Senescence
  • 批准号:
    10573323
  • 项目类别:
  • 资助金额:
    $69.39万
  • 财政年份:
    2022
  • 负责人:
    MARC Wallace KIRSCHNER
  • 依托单位:
海外基金