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TraPPs - Tracking of Phosphoinositide Pools - Key Signalling Components in Cell Migration and Polarisation

TraPPs - Tracking of Phosphoinositide Pools - Key Signalling Components in Cell Migration and Polarisation
TraPPs - 磷酸肌醇库的追踪 - 细胞迁移和极化中的关键信号成分
批准号:
128165748
负责人:
Professor Dr. Carsten Schultz
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2009
资助国家:
德国
项目状态:
已结题
起止时间:
2008-12-31 至 2011-12-31

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中文摘要
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英文摘要
Membrane dynamics modulate cell polarity, vesicular trafficking, migration, growth, proliferation, differentiation, and more. Of all membrane lipids, phosphoinositides play a central role in these processes (Wymann & Marone 2005 Curr Opin Cell Biol; Lindmo & Stenmark 2006 J Cell Sci; Simonsen & Stenmark 2007 Nat Chem Biol). Although a role for the prominent 3-phosphorylated phosphoinositides such as PtdIns(3,4,5)P3 and PtdIns(3)P has been highlighted in physiology and disease (Wymann et al. 2003 TiPS), dynamics and localization of these lipids are still poorly understood. TraPPs will provide a dynamic and refined view of phosphoinositide flux, and required lipid modifying enzymes, e.g. PI3Ks, lipases, and lipid phosphatases. Lipid-modifying enzymes will be targeted dynamically to distinct cellular locations, and lipid-interacting proteins shall be manipulated to display their free or lipid-bound state. Finally, the activity state of phospholipid-modifying enzymes will be imaged by the formation of enzyme-substrate complexes in living cells (Yudushkin et al., 2007, Science). Activation of lipid modifying enzymes will be linked to localized upstream signalling and specific cell responses. Cellular, genetic fly and mouse models will be used to validate the uncovered molecular mechanisms. This work provides the basis for a broader systems biology approach of lipid signaling, and will elucidate dynamic cellular processes relevant to cancer and inflammation.
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  • 批准号:
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  • 项目类别:
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  • 资助金额:
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    11176015
  • 项目类别:
    联合基金项目
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  • 批准年份:
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多流体ALE模式下Front tracking 界面追踪法研究