The goal of this proposal is to use cryo-electron microscopy to make three-dimensional reconstructions of COPII coated vesicles. COPII proteins are responsible for forming the vesicles that transport proteins and lipids from the endoplasmic reticulum (ER) to the Golgi apparatus. COPII proteins consist of Sar1, Sec23/24, and Sec13/31. These form a lattice on the ER membrane that invaginates the membrane into a spherical vesicle. Biochemical experiments have suggested ways that the proteins interact and have lead to a number of models for the formation of the COPII lattice. The structure of the COPII lattice will be studied by cryoelectron microscopy. Crystal structures of Sar1 and Sec23/24 have been solved. Fitting these structures into the reconstruction of the COPII coat will help determine the inter-protein contacts in the COPII lattice and how the lattice is formed. Moreover, these studies will contribute to the understanding of eukaryotic protein transport machinery and may contribute to the understanding and treatment of diseases associated with disrupted transport.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32GM073509-01
Application #
6884541
Study Section
Special Emphasis Panel (ZRG1-F04B (20))
Program Officer
Rodewald, Richard D
Project Start
2005-01-01
Project End
2006-12-31
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
1
Fiscal Year
2005
Total Cost
$48,296
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Stagg, Scott M; Lander, Gabriel C; Quispe, Joel et al. (2008) A test-bed for optimizing high-resolution single particle reconstructions. J Struct Biol 163:29-39
Stagg, Scott M; LaPointe, Paul; Razvi, Abbas et al. (2008) Structural basis for cargo regulation of COPII coat assembly. Cell 134:474-84
Stagg, Scott M; Lander, Gabriel C; Pulokas, James et al. (2006) Automated cryoEM data acquisition and analysis of 284742 particles of GroEL. J Struct Biol 155:470-81