Identification of synaptic alpha2delta binding partners

突触 alpha2delta 结合伙伴的鉴定

基本信息

  • 批准号:
    8597614
  • 负责人:
  • 金额:
    $ 25.35万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2013
  • 资助国家:
    美国
  • 起止时间:
    2013-06-01 至 2015-05-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Synapses represent key transduction machines that convert action potential-based signals into secreted chemical messages which in turn are converted back into postsynaptic electrical responses. Modulation of these processes is thought to underlie critical mechanisms of learning and memory, and dysfunction of synaptic communication is suspected to be central in a number of diseased states of brain function. It has long been known that the critical trigger for neurotransmitter release is the opening of voltage-gated calcium channels within the presynaptic terminal which in turn leads to the influx of calcium. The highly-non-linear relationship between calcium entry and exocytosis efficiency places the control of calcium channel function and abundance as a potent potential leverage point in sculpting synaptic strength. We recently demonstrated that expression of a calcium channel subunit, alpha2delta, is rate-limiting in determining how many calcium channels are present at nerve terminals in hippocampal neurons. Our work showed that it acts at 2 distinct molecular steps: it acts in a forward trafficking step to allow calcium channels to traffic to synapses and it acts locally at nerve terminals to allow channels to function at the presynaptic membrane. This second step requires the integrity of a predicted domain within alpha2delta that encodes a metal-ion-dependent adhesion site. In many other proteins this domain confers binding to an extracellular partner. We predict that proper alpha2delta function requires interaction with an as-yet-discovered binding partner on the synaptic surface. The goal of this proposal is to use biochemical approaches to identify this(ese) binding partner(s).
描述(由申请人提供):突触代表将基于动作电位的信号转换成分泌的化学信息的关键转导机器,所述化学信息又被转换回突触后电响应。这些过程的调节被认为是学习和记忆的关键机制的基础,并且突触通信功能障碍被怀疑是许多脑功能疾病状态的中心。长期以来,人们已经知道,神经递质释放的关键触发因素是突触前末梢内电压门控钙通道的开放,这反过来又导致钙的内流。钙进入和胞吐效率之间的高度非线性关系将钙通道功能和丰度的控制作为塑造突触强度的潜在杠杆点。我们最近证明,表达的钙通道亚基,α 2 δ,是限速在确定有多少钙通道是目前在海马神经元的神经末梢。我们的工作表明,它在2个不同的分子步骤中起作用:它在前向运输步骤中起作用,允许钙通道运输到突触,它在神经末梢局部起作用,允许通道在突触前膜起作用。这第二步需要在编码金属离子依赖性粘附位点的α 2 δ内的预测结构域的完整性。在许多其他蛋白质中,该结构域赋予与细胞外伴侣的结合。我们预测,适当的alpha2delta功能需要与突触表面上尚未发现的结合伴侣相互作用。该提案的目标是使用生物化学方法来鉴定这种(ese)结合伴侣。

项目成果

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Timothy Aidan Ryan其他文献

Timothy Aidan Ryan的其他文献

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{{ truncateString('Timothy Aidan Ryan', 18)}}的其他基金

Metabolic Vulnerability of Synapses in Neurodegenerative Disease
神经退行性疾病中突触的代谢脆弱性
  • 批准号:
    10578785
  • 财政年份:
    2020
  • 资助金额:
    $ 25.35万
  • 项目类别:
Metabolic Vulnerability of Synapses in Neurodegenerative Disease
神经退行性疾病中突触的代谢脆弱性
  • 批准号:
    10365919
  • 财政年份:
    2020
  • 资助金额:
    $ 25.35万
  • 项目类别:
Identification of synaptic alpha2delta binding partners
突触 alpha2delta 结合伙伴的鉴定
  • 批准号:
    8660359
  • 财政年份:
    2013
  • 资助金额:
    $ 25.35万
  • 项目类别:
Development of a Synaptic ATP Reporter
突触 ATP 报告基因的开发
  • 批准号:
    8066969
  • 财政年份:
    2010
  • 资助金额:
    $ 25.35万
  • 项目类别:
Development of a Synaptic ATP Reporter
突触 ATP 报告基因的开发
  • 批准号:
    7977318
  • 财政年份:
    2010
  • 资助金额:
    $ 25.35万
  • 项目类别:
Quantitative Mapping of Molecules and Release Properties at Nerve Terminals
神经末梢分子和释放特性的定量图谱
  • 批准号:
    7781100
  • 财政年份:
    2009
  • 资助金额:
    $ 25.35万
  • 项目类别:
Quantitative mapping of molecules and release properties at nerve terminals
神经末梢分子和释放特性的定量图谱
  • 批准号:
    8825287
  • 财政年份:
    2009
  • 资助金额:
    $ 25.35万
  • 项目类别:
Quantitative Mapping of Molecules and Release Properties at Nerve Terminals
神经末梢分子和释放特性的定量图谱
  • 批准号:
    8586902
  • 财政年份:
    2009
  • 资助金额:
    $ 25.35万
  • 项目类别:
Quantitative Mapping of Molecules and Release Properties at Nerve Terminals
神经末梢分子和释放特性的定量图谱
  • 批准号:
    8389677
  • 财政年份:
    2009
  • 资助金额:
    $ 25.35万
  • 项目类别:
Quantitative Mapping of Molecules and Release Properties at Nerve Terminals
神经末梢分子和释放特性的定量图谱
  • 批准号:
    8196919
  • 财政年份:
    2009
  • 资助金额:
    $ 25.35万
  • 项目类别:

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