Mechanisms of signal-dependent photoreceptor protein localization and transport

信号依赖性光感受器蛋白定位和运输机制

• 批准号: 7683195
• 负责人: Peter Deane Calvert
• 金额: $ 35.33万
• 依托单位: UPSTATE MEDICAL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-01 至 2012-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7683195
• 关键词: Arrestins; Behavior; Degenerative Disorder; Disease; Eye; Green Fluorescent Proteins; Lead; Learning; Life; Light; Lighting; Methods; Microscopy; Modeling; Pattern; Photophobia; Photoreceptors; Play; Proteins; Retinal Degeneration; Retinal Diseases; Role; Signal Transduction; Signaling Molecule; Testing; Therapeutic Intervention; Transducin; Variant; Vision research; Work; design; experience; photoreceptor degeneration; programs; protein transport; recoverin protein; research study; retinal rods; sensor

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.

描述（由申请人提供）：视网膜视杆细胞中涉及光信号传导的三种高度表达的蛋白质，transducin、recoverin和arrestin，根据环境照明条件定位于不同的光感受器隔室。这种转运对于调节感光器的光敏感性是重要的。此外，它在保护视杆光感受器免受我们每天经历的光水平的持续刺激引起的损伤以及可能导致许多先天性视网膜退行性疾病的异常光感受器活性方面发挥作用。然而，这些蛋白质被定位到光感受器隔室的机制，它们在隔室之间运输的机制，以及环境光水平的变化引发这种重新定位的机制尚不清楚。 我们已经开发了新的方法，使用多光子显微镜直接检查蛋白质的局部，区室特异性行为和活的，功能性光感受器内信号分子的局部变化。使用这些新方法，我们将检查： 目的1：蛋白质定位于视杆细胞的机制。 目的2：视杆细胞间的信号依赖性蛋白质转运模式。 目的3：启动蛋白质转运的信号。 目标1和2中的实验将定量检查与绿色荧光蛋白的变体（可光活化GFP）融合的蛋白质的局部和长距离迁移率，以鉴定定位机制和运输模式。然后，我们将采取我们从这些研究中学到的知识，并构建一个定量模型来测试迁移率参数是否足以解释蛋白质定位和光驱动运输的模式。目标3中的实验设计用于识别使用新开发的、可表达的信号转导传感器告诉蛋白质移动的信号。 了解光诱导蛋白质转运的机制可以揭示直接测试转运的适应性或保护作用的实验策略，并可能导致治疗干预策略，以减缓或逆转先天性疾病中的光感受器变性。这项工作符合视网膜疾病计划下的国家眼睛和视力研究计划。