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CORE--TECHNICAL SUPPORT

CORE--TECHNICAL SUPPORT
核心--技术支持
批准号:
6336675
负责人:
Archibald S. Perkins
金额:
$30.98万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-08-01 至 2001-07-31

项目摘要

项目成果

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中文摘要
翻译
技术核心将提供三大职能,协助方案规划小组的四个项目。它们是蛋白质纯化、蛋白质表达分析和基因表达分析。这些系统的组成部分概述如下,包括支助人员和设备。技术核心将促进下面描述的每个项目的进展,以及组成计划项目的五个实验室之间的互动。1.蛋白质纯化:FPLC。珀金夫妇目前有一个用于蛋白质纯化的FPLC,这将成为技术支持核心的一部分。克劳斯的项目(项目2)将利用这一点来纯化与CD34启动子上游调控区域结合的因子。Weissman的项目(特定目标4)也将使用它来识别与中性粒细胞激活下调的基因上游调控序列结合的蛋白质。由于FPLC已经在现场,我们只请求需要的额外列。2.蛋白质表达分析A.二维凝胶:设备、用品、技术员(郑博士)和Melanie II软件B.MALDI-MS:技术员)Edward Papacoda)。这一PPG的一个关键的压倒一切的主题是分析骨髓生成过程中的造血细胞的分子解剖学,包括初始阶段(项目2),以及正常和表达EVI-1的细胞的诱导成熟(项目3),以及对大肠杆菌的反应(项目4)。这些项目将研究信使核糖核酸水平(见下一节)和蛋白质水平的变化。分子生物学中最令人兴奋的新发展之一是能够通过胰酶消化和质谱学来识别蛋白质,使用MALDI-MS(基质辅助激光解吸/电离质谱仪)与ProSite软件相结合来搜索蛋白质和DNA序列数据库。这使得可以使用低至10fmol的蛋白质来识别蛋白质,这不到50,000道尔顿蛋白质的1 ng(相当于银染凝胶上可检测到的下限)。与此同时,蛋白质二维凝胶分析的硬件和软件也得到了改进,允许对蛋白质进行可重复的分级,并对不同的凝胶进行详细比较,以确定数量差异。我们打算充分利用这些进展,并要求资金购买设备、用品和技术支持,使我们能够做到这一点。这一核心设施将积累的信息和专门知识将使这一项目组合中的所有项目大大受益,并为其提供有力的支持。3.基因表达分析A.Affymetrix基因芯片技术B.差异显示3.序列分析在mRNA差异分析项目中的共同主题将得到技术核心的三个关键组成部分的支持。Affymetrix基因芯片分析系统可以评估数千种不同小鼠基因的表达水平。目前,在四个芯片上可以获得6500个老鼠基因。这些基因在硅芯片上以微阵列的形式存在,并使用计算机芯片制造中使用的标准DNA合成化学和掩蔽技术进行原位合成。以感兴趣的mRNA为模板,将这些阵列与荧光标记的cDNA杂交,并通过扫描激光进行杂交。Affymetrix系统由五个组件组成:基因芯片探针阵列、基因芯片流体站400、惠普基因阵列扫描仪和基因芯片探针阵列、基因芯片软件。总而言之,该系统实现了杂交、洗涤以及数据捕获和分析中的许多步骤的自动化。
英文摘要
The Technical Core will provide three broad functions that will assist the four Projects of the PPG. These are Protein Purification, Protein Expression Analysis, and Gene Expression Analysis. The components of these are outlined below, and include both support personnel and equipment. The Technical Core will facilitate the progress of each project as described below, as well ss interaction between the five labs comprising the Program Project. 1. Protein purification: FPLC. The Perkins currently has an FPLC for protein purification, and this will become part of the Technical Support Core. This will be utilized by Krause's project (Project 2) to purify the factor that binds to the upstream regulatory region of the CD34 promoter. It will also be used by Weissman's project (Specific Aim 4) to identify the proteins that bind to upstream regulatory sequences of genes that are down- regulated on neutrophil activation. Since the FPLC is already on site, we only requesting additional columns that are needed. 2. Protein expression analysis A. 2d-GELS: Equipment,, supplies, technician (Dr. Zheng) and Melanie II software B. MALDI-MS: Technician )Edward Papacoda). A key overriding theme to this PPG is the analysis of the Molecular Anatomy of hematopoietic cells during the process of myelopoiesis, including the initial stages (Project 2), as well as in induced maturation in normal and EVI-1-expressing cells (Project 3), and in response to E. coli (Project 4). These projects will examine changes in both the mRNA level (see next section) and the protein level. One of the most exciting new developments in molecular biology is the ability to identify proteins by tryptic digest and mass spectrometry, using the MALDI-ms (matrix-assisted laser desorption/ionization mass spectrometry) in conjunction with the Prosite software for searching protein and DNA sequence databases. This has allowed the identification of proteins using as little as 10 fmol, which is less than 1 ng of a 50,000 dalton protein (equivalent to the lower limit of what is detectable on silver-stained gels). In parallel, hardware and software for 2D gel analysis of proteins has improved, to allow reproducible fractionation of proteins, and detailed comparison of different gels to identify quantitative differences. We intend to take full advantage of these advances, and are requesting money for equipment, supplies, and technical support to enable us to do this. The cumulative accrual of information and expertise that will occur with this core facility will substantially benefit all of the projects in this PPG, and provides a cogent argument in its support. 3. Gene expression analysis A. Affymetrix gene chip technology B. Differential Display 3. Sequence analysis The common theme among the projects of mRNA difference analysis will be supported by three key components of the Technical Core. The Affymetrix GeneChip analysis system allows the assessment of expression levels for thousands of different mouse genes. At present, 6,500 mouse genes are available on four chips. These genes are present as microarrays on a silica chip and are synthesized in situ using standard DNA synthesis chemistry as well as masking technology utilized in computer chip manufacturing. The arrays are hybridized with fluorescently labeled cDNA, using the mRNA of interest as a template, and the hybridization is "read" by a scanning laser. The Affymetrix system consists of five components: the GeneChip Probe Array, GeneChip Fluidics Station 400, Hewlett-Packard GeneArray Scanner, and GeneChip Probe Array, Gene Chip Software. Together, this system has automated many steps in the hybridization, washing, and data capture and analysis.
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Function of the PR domain of the MDSI-EVI1 in MLL fusion protein leukemogenesis
  • 批准号:
    8697619
  • 项目类别:
  • 资助金额:
    $31.85万
  • 财政年份:
    2014
  • 负责人:
    Archibald S. Perkins
  • 依托单位:
Mechanism of EVI1-induced Leukemogenesis
  • 批准号:
    7901430
  • 项目类别:
  • 资助金额:
    $32.08万
  • 财政年份:
    2007
  • 负责人:
    Archibald S. Perkins
  • 依托单位:
Mechanism of EVI1-induced Leukemogenesis
  • 批准号:
    7319762
  • 项目类别:
  • 资助金额:
    $32.96万
  • 财政年份:
    2007
  • 负责人:
    Archibald S. Perkins
  • 依托单位:
Mechanism of EVI1-induced Leukemogenesis
  • 批准号:
    7496113
  • 项目类别:
  • 资助金额:
    $33.84万
  • 财政年份:
    2007
  • 负责人:
    Archibald S. Perkins
  • 依托单位:
海外基金