课题基金 / 基金详情

Determining the Structural Topology of Nephrin-Receptor-Signaling-Complexes

Determining the Structural Topology of Nephrin-Receptor-Signaling-Complexes
确定去氧肾上腺素受体信号复合物的结构拓扑
批准号:
8538371
负责人:
Chi Won Pak
金额:
$5.39万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-01 至 2014-08-31

项目摘要

项目成果

Chi Won Pak的其他基金

相关文献

中文摘要
翻译
说明书(由申请人提供):newitin发出的信号需要接头蛋白Nck和肌动蛋白成核促进因子N-WASP来刺激有效的肾小球功能所必需的肌动蛋白聚合。这一信号通路的中断会导致肾病综合征,其特征是蛋白异常分泌到尿液中,最终导致终末期肾功能衰竭。蛋白质的聚集性对于有效的信号传递是很重要的,尽管还缺乏机制上的理论基础。我们实验室的研究发现了一种通过二聚化来调节N-WASP活性的新方法,它可以将N-WASP的体外活性提高100倍。我们假设NCK聚簇调节N-WASP二聚体在neparin信号中的作用,这是我们打算研究的。
英文摘要
DESCRIPTION (provided by applicant): Signaling by nephrin requires the adaptor protein, Nck, and the actin nucleation-promoting factor, N-WASP, to stimulate actin polymerization necessary for efficient glomerular function. Disruptions to this signaling pathway result in nephrotic syndromes, which are characterized by abnormal secretion of protein into urine and ultimately end-stage renal failure. Clustering of the proteins, nephrin and Nck, have been suggested to be important for efficient signaling, though a mechanistic rationale for this is lacking. Studies from our lab have identified a novel regulation of N-WASP activity through dimerization, which increases N-WASP's activity in vitro by >100- fold. We hypothesize that Nck clustering regulates N-WASP dimerization in nephrin signaling, which we propose to study.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Determining the Structural Topology of Nephrin-Receptor-Signaling-Complexes
  • 批准号:
    8325835
  • 项目类别:
  • 资助金额:
    $5.22万
  • 财政年份:
    2011
  • 负责人:
    Chi Won Pak
  • 依托单位:
Determining the Structural Topology of Nephrin-Receptor-Signaling-Complexes
  • 批准号:
    8203019
  • 项目类别:
  • 资助金额:
    $4.84万
  • 财政年份:
    2011
  • 负责人:
    Chi Won Pak
  • 依托单位: