Determinants of Rod and Cone Response Characteristics
杆和锥响应特性的决定因素
基本信息
- 批准号:6649367
- 负责人:
- 金额:$ 37.4万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1986
- 资助国家:美国
- 起止时间:1986-07-01 至 2006-06-30
- 项目状态:已结题
- 来源:
- 关键词:arrestins cone cell dark adaptation electrophysiology electroretinography flow cytometry genetically modified animals high performance liquid chromatography laboratory mouse light adaptations mass spectrometry phosphorylation polymerase chain reaction protein structure function rhodopsin rhodopsin kinase rod cell transducin visual photoreceptor visual photosensitivity visual phototransduction visual pigments
项目摘要
DESCRIPTION (provided by applicant): Photoreceptors have several important
physiological functions. They detect light but they also adapt to constant
illumination and darkness. Phosphorylation of rhodopsin is a critical
biochemical reaction that modulates the phototransduction cascade. In this
proposal we outline methods to precisely characterize the contributions of
rhodopsin phosphorylation to light and dark adaptation and to the kinetics of
the photoresponse. Rhodopsin phosphorylation will be measured both in isolated
intact mouse retinas and in vivo using high-resolution rapid quench and mass
spectrometry methodology. The time course of rhodopsin phosphorylation will be
established under a variety of physiologically important conditions.
Physiological responses of rod photoreceptors will be established by
quantitative electroretinography under conditions identical to those used for
phosphorylation measurements. A variety of mouse strains will be examined in
which genes encoding proteins that influence rhodopsin phosphorylation and
regeneration are mutated. Retinoid metabolism will be monitored and it will
also be compared with the kinetics of physiological responses to light and
darkness. These studies will precisely define the contributions of
phosphorylation and visual cycle reactions to light and dark adaptation and
photoresponse kinetics in mammalian retinas.
描述(由申请人提供):光感受器具有几个重要的
生理功能。它们能探测到光线,
照明和黑暗。视紫红质的磷酸化是
调节光传导级联的生化反应。在这
建议我们概述的方法,以准确描述的贡献,
视紫红质磷酸化对光和暗适应的影响以及对
光反应。视紫红质磷酸化将在分离的
完整小鼠视网膜和体内使用高分辨率快速淬灭和质量
光谱测定法视紫红质磷酸化的时间过程将是
在各种生理学上重要的条件下建立。
视杆细胞光感受器的生理反应将通过
定量视网膜电图,条件与用于
磷酸化测量。将对各种小鼠品系进行检查,
哪些基因编码影响视紫红质磷酸化的蛋白质,
再生是变异的。将监测类维生素A代谢,
也可以与对光的生理反应的动力学进行比较,
山中贼易这些研究将准确地确定
磷酸化和视觉周期反应的光和暗适应,
哺乳动物视网膜的光反应动力学。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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JAMES Bryant HURLEY其他文献
JAMES Bryant HURLEY的其他文献
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{{ truncateString('JAMES Bryant HURLEY', 18)}}的其他基金
Enhancing cone survival in retinitis pigmentosa through cell-specific therapeutic CRISPR editing of a roxadustat target
通过 roxadustat 靶标的细胞特异性治疗性 CRISPR 编辑来增强色素性视网膜炎中视锥细胞的存活
- 批准号:
10624450 - 财政年份:2022
- 资助金额:
$ 37.4万 - 项目类别:
Enhancing cone survival in retinitis pigmentosa through cell-specific therapeutic CRISPR editing of a roxadustat target
通过 roxadustat 靶标的细胞特异性治疗性 CRISPR 编辑来增强色素性视网膜炎中视锥细胞的存活
- 批准号:
10421156 - 财政年份:2022
- 资助金额:
$ 37.4万 - 项目类别:
HYBRID STRUCTURE DETERMINATION OF TRAFFICKING COMPLEXES BY SAXS, CRYSTALLOGRAPHY
通过 SAXS、晶体学测定贩运复合物的混合结构
- 批准号:
8362155 - 财政年份:2011
- 资助金额:
$ 37.4万 - 项目类别:
HYBRID STRUCTURE DETERMINATION OF TRAFFICKING COMPLEXES BY SAXS, CRYSTALLOGRAPHY
通过 SAXS、晶体学测定贩运复合物的混合结构
- 批准号:
8170103 - 财政年份:2010
- 资助金额:
$ 37.4万 - 项目类别:
HYBRID STRUCTURE DETERMINATION OF TRAFFICKING COMPLEXES BY SAXS, CRYSTALLOGRAPHY
通过 SAXS、晶体学测定贩运复合物的混合结构
- 批准号:
7954430 - 财政年份:2009
- 资助金额:
$ 37.4万 - 项目类别:
HYBRID STRUCTURE DETERMINATION OF TRAFFICKING COMPLEXES BY SAXS, PROTEIN CRYSTAL
通过 SAXS、蛋白质晶体测定贩运复合物的混合结构
- 批准号:
7722121 - 财政年份:2008
- 资助金额:
$ 37.4万 - 项目类别: