Dynamics of Endomembrane Docking and Fusion

内膜对接和融合的动力学

• 批准号: 10386618
• 负责人: Alexey Jarrell Merz
• 金额: $ 20.93万
• 依托单位: UNIVERSITY OF WASHINGTON
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-03-01 至 2025-03-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10386618
• 关键词: Antibodies; Biochemical; Biological Assay; Cell Extracts; Cell physiology; Chemicals; Consumption; Disease; Docking; Genes; Golgi Apparatus; Grant; HIV; Hormone secretion; Lesion; Lipids; Measures; Mediating; Membrane Protein Traffic; Pathway interactions; Proteins; Public Health; System; Testing; Vesicle; Virus Assembly; Virus Diseases; fundamental research; human disease; reconstitution; therapeutic development; virus genetics

Abstract Summary COPII mediated ER-to-golgi membrane traffic was first reconstituted using crude cell extracts thirty years ago. Twenty years ago, the formation of COPII vesicles was recapitulated using pure proteins and lipids. However, the consumption of COPII vesicles – their uncoating, tethering, docking, and fusion with accep- tor compartments, is still poorly understood. This is in large measure because the crude transport assay developed thirty years ago has not been supplanted by a system employing chemically defined components. In this Project we introduce such a system and use it to test hypotheses about the sequence of biochemical subreactions in COPII vesicle traffic, the components that execute these subreactions, and the mechanisms through which they function.

摘要摘要 Copii介导的ER到高尔基膜交通首先使用三十年的粗细细胞提取物重构 前。二十年前，使用纯蛋白和脂质概括了Copii蔬菜的形成。 但是，食用Copii蔬菜 - 它们的脱衣，束缚，对接和融合与接受 - TOR隔室，仍然很了解。这是大量测量的，因为原油运输测定法 开发的30年前并未被采用化学定义组件的系统所取代。 在这个项目中，我们介绍了这样的系统，并使用它来测试有关生化序列的假设 COPII场地流量中的子配置，执行这些子反应的组件以及机制 通过它们的功能。