PROTEIN TRANSPORT INTO MAMMALIAN ENDOPLASMIC RETICULUM

蛋白质转运至哺乳动物内质网

• 批准号: 6386151
• 负责人: Tom A Rapoport
• 金额: $ 22.11万
• 依托单位: HARVARD MEDICAL SCHOOL
• 依托单位国家: 美国
• 财政年份: 1995
• 资助国家: 美国
• 起止时间: 1995-05-01 至 2003-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6386151
• 关键词: crosslink; dogs; electron microscopy; endoplasmic reticulum; membrane biogenesis; membrane channels; membrane proteins; protein biosynthesis; protein protein interaction; protein reconstitution; protein signal sequence; protein structure function; protein transport; ribosomes; secretory protein

The long-term goal of this project is to understand the molecular mechanism by which proteins are transported across or are inserted into the mammalian endoplasmic reticulum (ER) membrane. We have established reconstituted proteoliposome and soluble systems with purified membrane protein components which reproduce the overall translocation process and partial reactions. The minimum translocation apparatus of the ER membrane comprises only the heterotrimeric Sec61p complex, the TRAM protein, and the SRP receptor. We now propose to perform a thorough analysis of the mechanism of translocation. Specifically, we will use questions: 1. How is cotranslational translocation initiated? 2. How do ribosomes interact with the Sec61p channel? 3. How are membrane proteins inserted into the lipid bilayer? 4. What is the function of the mammalian homologs of Sec62p and Sec63p? These studies will contribute significantly to our understanding of the first and decisive step in the biosynthesis of a large of class proteins, proteins of the plasma membrane, of lysosomes, and of all organelles of the secretory pathway.

该项目的长期目标是了解蛋白质在哺乳动物内质网（ER）膜上运输或插入的分子机制。我们已经建立了重组的蛋白脂质体和可溶性系统，纯化的膜蛋白组分再现了整个易位过程和部分反应。内质网膜的最小易位装置仅包括异三聚体Sec61p复合体、TRAM蛋白和SRP受体。我们现在建议对易位的机制进行彻底的分析。具体来说，我们将使用以下问题：共译易位是如何开始的？2. 核糖体如何与Sec61p通道相互作用？3. 膜蛋白如何插入脂质双分子层？4. Sec62p和Sec63p的哺乳动物同源物的功能是什么？这些研究将大大有助于我们理解生物合成大量蛋白质的第一步和决定性步骤，质膜蛋白质，溶酶体蛋白质，以及分泌途径的所有细胞器。