课题基金 / 基金详情

项目摘要

项目成果

Peter Deane Calvert的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Three highly expressed proteins involved in light signaling in retinal rod photoreceptors, transducin, recoverin and arrestin, localize to different photoreceptor compartments depending on the conditions of ambient illumination. This transport is important for adjusting photoreceptor light sensitivity. Moreover, it plays a role in protecting rod photoreceptors from damage caused by continual stimulation from light levels we experience every day, and from aberrant photoreceptor activity that may underlie many congenital retinal degenerative diseases. Yet the mechanisms by which these proteins are localized to photoreceptor compartments, by which they are transported among compartments and by which changes in ambient light levels initiate this re-localization are not known. We have developed new methods using multiphoton microscopy to directly examine local, compartment-specific behavior of the proteins and local changes in signaling molecules within living, functioning photoreceptors. Using these new methods we will examine the: Aim 1: Mechanisms underlying protein localization to rod photoreceptor compartments. Aim 2: Mode of signal-dependant protein transport between rod compartments. Aim 3: Signals that initiate protein transport. Experiments in aims 1 and 2 will quantitatively examine the local and long distance mobilities of the proteins fused with a variant of the green fluorescent protein, photoactivatable GFP, to identify the mechanisms of localization and modes of transport. We will then take what we have learned from these studies and construct a quantitative model to test if the mobility parameters are sufficient to explain the patterns of protein localization and light-driven transport. Experiments in aim 3 are designed to identify the signals that tell the proteins to move using newly developed, expressible signal transduction sensors. Understanding the mechanisms of light-induced protein transport could reveal experimental strategies for testing adaptive or protective roles of transport directly and may lead to strategies for therapeutic intervention to slow or reverse photoreceptor degeneration in congenital disease. The proposed work fits into the National Plan for Eye and Vision Research under the Retinal Disease Program.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Construction and stability of photoreceptor outer segment discs
  • 批准号:
    10091444
  • 项目类别:
  • 资助金额:
    $42.88万
  • 财政年份:
    2018
  • 负责人:
    Peter Deane Calvert
  • 依托单位:
Construction and stability of photoreceptor outer segment discs
  • 批准号:
    10357735
  • 项目类别:
  • 资助金额:
    $42.88万
  • 财政年份:
    2018
  • 负责人:
    Peter Deane Calvert
  • 依托单位:
Mechanisms of signal-dependent photoreceptor protein localization and transport
  • 批准号:
    8123268
  • 项目类别:
  • 资助金额:
    $33.91万
  • 财政年份:
    2007
  • 负责人:
    Peter Deane Calvert
  • 依托单位:
Mechanisms of photoreceptor protein transport and compartmentalization
  • 批准号:
    10536598
  • 项目类别:
  • 资助金额:
    $50.59万
  • 财政年份:
    2007
  • 负责人:
    Peter Deane Calvert
  • 依托单位:
国内基金
海外基金
AT1R-G蛋白/β-arrestins通路偏好性激活在急性肾损伤中的作用及其机制
  • 批准号:
    82104272
  • 项目类别:
    青年科学基金项目(C类)
  • 资助金额:
    30.0万元
  • 批准年份:
    2021
  • 负责人:
    贾英丽
  • 依托单位:
催产素受体Gαq与β-arrestins偏爱型信号通路在产后抑郁症中的作用
  • 批准号:
    82104148
  • 项目类别:
    青年科学基金项目(C类)
  • 资助金额:
    30.0万元
  • 批准年份:
    2021
  • 负责人:
    朱佳蕾
  • 依托单位:
β-arrestins在DC细胞迁移及自身免疫疾病中的作用及机制研究
  • 批准号:
    31871404
  • 项目类别:
    面上项目
  • 资助金额:
    60.0万元
  • 批准年份:
    2018
  • 负责人:
    杜昌升
  • 依托单位:
β-arrestins调节小胶质细胞M1/M2表型转化及其在阿尔兹海默病进程中的作用
  • 批准号:
    81703488
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.1万元
  • 批准年份:
    2017
  • 负责人:
    方吟荃
  • 依托单位: