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 recently established a system of reconstituted proteoliposomes which reproduces the translocation process with purified membrane proteins and pure phospholipids. The minimum translocation apparatus of the ER membrane seems to comprise only the Sec61p- complex of three subunits and the TRAM protein. We now propose to thoroughly analyze the mechanism of translocation, in terms of these individual components. Specifically, we will use crosslinking and reconstitution methods to address the following questions: 1. What are the steps of translocation on a molecular level? 2. What are the functions of the Sec61p- complex? 3. How does the TRAM protein facilitate translocation? We will also search for additional components which may be required for the postranslational mode of translocation, for the recycling of translocation components and for the regulation of the translocation process. We believe that our studies will contribute significantly to the understanding of the first and decisive step in the biosynthesis of a large class of proteins which includes secretory proteins, proteins of the plasma membrane, of lysosomes and of all organelles of the secretory pathway.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM052586-01
Application #
2191673
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1995-05-01
Project End
1999-04-30
Budget Start
1995-05-01
Budget End
1996-04-30
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Harvard University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
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Rapoport, Tom A; Li, Long; Park, Eunyong (2017) Structural and Mechanistic Insights into Protein Translocation. Annu Rev Cell Dev Biol 33:369-390
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Baldridge, Ryan D; Rapoport, Tom A (2016) Autoubiquitination of the Hrd1 Ligase Triggers Protein Retrotranslocation in ERAD. Cell 166:394-407
Li, Long; Park, Eunyong; Ling, JingJing et al. (2016) Crystal structure of a substrate-engaged SecY protein-translocation channel. Nature 531:395-399
Tan, Dongyan; Blok, Neil B; Rapoport, Tom A et al. (2016) Structures of the double-ring AAA ATPase Pex1-Pex6 involved in peroxisome biogenesis. FEBS J 283:986-92

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