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中文摘要
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描述(由申请人提供):在过去的十年中,成像、分子生物学和生物化学取得了惊人的进展,使单个蛋白质在体内的行为可视化。在这里,我建议开发和可视化的时间和空间动态的活神经元内的细胞内信号。就像早期的钙成像工作通过定义其空间和时间特征重新定义了我们对钙内流重要性的理解一样,我相信可视化细胞内信号的空间和时间动力学对我们理解神经系统也有类似的好处。最初,我们已经开发出能够可视化许多细胞内信号级联的关键第一步之一的指标:酪氨酸磷酸化。在过去的几年中,我们已经开发出一种系统,依赖于比率成像的变化,在基因编码的荧光指示剂磷酸化。我们现在提出了三个具体的目标,将这些工具开发成一个系统,用于监测神经元可塑性和发育过程中的信号传导。我们建议:1)开发针对报告特定激酶活性的指标库; 2)开发定位于特定细胞区室的指标; 3)开发同时报告多种信号分子活性的指标。使用我们的指标,工作人员将能够阐明突触可塑性基础的信号动力学。因此,我们的工具将使新的见解的基本机制,神经元可塑性的基础。公共卫生相关性:神经元可塑性是大脑中许多基本功能的基础,而异常的神经元可塑性与疾病有关。过度的可塑性可能是癫痫和成瘾等疾病的基础,而可塑性的缺陷可能在癫痫,神经退行性疾病和自闭症谱系障碍中发挥重要作用。我们的研究将通过开发新的工具来可视化具有亚细胞分辨率的动态神经元信号传导,从而在所有这些水平上产生广泛的影响。
英文摘要
DESCRIPTION (provided by applicant): During the past decade stunning advances have been made in imaging, molecular biology and biochemistry that enable the visualization of the behavior of single proteins in vivo. Here, I propose to develop and visualize the temporal and spatial dynamics of intracellular signaling within living neurons. Much as early work in calcium imaging redefined our understanding of the importance of calcium influx by defining its spatial and temporal characteristics, I believe visualizing the spatial and temporal dynamics of intracellular signaling will have similar benefits to our understanding of the nervous system. Initially we have developed indicators that enable visualization of one of the key first steps in many intracellular signaling cascades: tyrosine phosphorylation. During the past several years, we have developed a system that relies on ratiometric imaging of changes in a genetically encoded fluorescent indicator of phosphorylation. We now propose three specific aims to develop these tools into a system for monitoring signaling during neuronal plasticity and development. We propose to: 1) Develop a library of indicators targeted to report activity of specific kinases; 2) Develop indicators that localize to specific cellular compartments; 3) Develop indicators to report activity of multiple signaling molecules simultaneously. Using our indicators, workers will be able to elucidate the dynamics of signals that underlie synaptic plasticity. Thus, our tools will enable novel insights into essential mechanisms that underlie neuronal plasticity. PUBLIC HEALTH RELEVANCE: Project Narrative Neuronal plasticity underlies many fundamental functions within the brain, while abnormal neuronal plasticity is associated with disease. Excessive plasticity may underlie diseases like epilepsy and addiction, while defects in plasticity could play important roles in epilepsy, neurodegenerative, and autism spectrum disorders. Our research will have broad impacts across all these levels by developing new tools to visualize dynamic neuronal signaling with subcellular resolution.
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Novel mechanisms regulating protein interaction and pain
  • 批准号:
    10350573
  • 项目类别:
  • 资助金额:
    $51.41万
  • 财政年份:
    2019
  • 负责人:
    Matthew B Dalva
  • 依托单位:
Extracellular mechanism regulating synaptic function and pain plasticity
  • 批准号:
    10226181
  • 项目类别:
  • 资助金额:
    $51.11万
  • 财政年份:
    2019
  • 负责人:
    Matthew B Dalva
  • 依托单位:
Extracellular mechanism regulating synaptic function and pain plasticity
  • 批准号:
    10675034
  • 项目类别:
  • 资助金额:
    $51.11万
  • 财政年份:
    2019
  • 负责人:
    Matthew B Dalva
  • 依托单位:
Extracellular mechanism regulating synaptic function and pain plasticity
  • 批准号:
    10001045
  • 项目类别:
  • 资助金额:
    $51.11万
  • 财政年份:
    2019
  • 负责人:
    Matthew B Dalva
  • 依托单位:
海外基金