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ANNEXIN PHOSPHORYLATION: CAUSES AND CONSEQUENCES

ANNEXIN PHOSPHORYLATION: CAUSES AND CONSEQUENCES
膜联蛋白磷酸化:原因和后果
批准号:
6685899
负责人:
CARL E CREUTZ
金额:
$22.1万
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:
2000-12-15 至 2006-11-30

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DESCRIPTION (Applicant's abstract): The annexins are calcium-dependent, phospholipid-binding proteins that are the major peripheral proteins that move on and off membranes in response to calcium signalling events in cells. Evidence suggests they regulate a number of enzyme activities on membranes such as protein kinases and phospholipases, they act as receptors and docking sites for other proteins on the membrane, and they may mediate membrane-membrane interactions underlying exocytosis, endocytosis, and organelle tra.fficking. A number of annexins are phosphorylated in response to cell stimulation by secretogogues, growth factors, and oncogenic kinases. This project seeks to understand the most important ftinctions of annexins by identifying the physiological and pathological conditions under which they are phosphorylated, the protein kinases involved, and the consequences of the phosphorylation in terms of the regulation of cellular activities. The structure of annexin VI with a mutation that mimics phosphorylation will be determined by X-ray crystallography. The conformation of native and mutant annexin VI on lipid monolayers will be determined by electron microscopy of 2 dimensional crystals. Proteins that dock onto the phosphorylation sites on annexins will be characterized. The influence of phosphorylation on the locations and movements of annexins in cells will be determined, including the movements of annexins into the nucleus of the cell. These fundamental studies on the organization of membranes and their associated proteins should lead to a better understanding of cell signalling events that underlie the release of hormones and neurotransmitters and the regulation of cell growth under normal and pathological conditions.
期刊论文(3)
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会议论文
Novel protein ligands of the annexin A7 N-terminal region suggest pro-beta helices engage one another with high specificity.
膜联蛋白 A7 N ​​末端区域的新型蛋白质配体表明 pro-β 螺旋以高度特异性相互结合。
DOI: --
发表时间: 2009
期刊: General physiology and biophysics
影响因子: 1.5
作者: [Creutz,CarlE]
通讯作者: Creutz,CarlE
Structural and dynamic changes in human annexin VI induced by a phosphorylation-mimicking mutation, T356D.
由磷酸化模拟突变 T356D 诱导的人膜联蛋白 VI 的结构和动态变化。
DOI: 10.1021/bi026742h
发表时间: 2003
期刊: Biochemistry.
影响因子: --
作者: [Freye-Minks,Caroline, Kretsinger,RobertH, Creutz,CarlE]
通讯作者: Creutz,CarlE
Atomic Force Microscope
  • 批准号:
    7792772
  • 项目类别:
  • 资助金额:
    $20.33万
  • 财政年份:
    2010
  • 负责人:
    CARL E CREUTZ
  • 依托单位:
ANNEXIN PHOSPHORYLATION: CAUSES AND CONSEQUENCES
  • 批准号:
    6266303
  • 项目类别:
  • 资助金额:
    $22.11万
  • 财政年份:
    2000
  • 负责人:
    CARL E CREUTZ
  • 依托单位:
ANNEXIN PHOSPHORYLATION: CAUSES AND CONSEQUENCES
  • 批准号:
    6625108
  • 项目类别:
  • 资助金额:
    $22.1万
  • 财政年份:
    2000
  • 负责人:
    CARL E CREUTZ
  • 依托单位:
ANNEXIN PHOSPHORYLATION: CAUSES AND CONSEQUENCES
  • 批准号:
    6476562
  • 项目类别:
  • 资助金额:
    $22.1万
  • 财政年份:
    2000
  • 负责人:
    CARL E CREUTZ
  • 依托单位:
国内基金
海外基金
D型IC-8多肽修饰的还原敏感型RHB自组装双靶向核酸递送载体的研究
  • 批准号:
    81273459
  • 项目类别:
    面上项目
  • 资助金额:
    60.0万元
  • 批准年份:
    2012
  • 负责人:
    沙先谊
  • 依托单位: