The broad objective of the proposed research is to understand the enzymology of transport of proteins between cellular organelles of the secretory pathway of eucaryotic cells. The biochemical basis for transport of a plasma-membrane protein from the endoplasmic reticulum (ER) to the Golgi will be studied using a model system based on the G protein of vesicular stomatitis virus (VSV) in infected Chinese hamster ovary (CHO) cells. Transport will be studied using a newly developed in vitro assay which measures the export of the temperature-sensitive mutant VSV strain ts045 G protein from the ER to the cis compartment of the Golgi containing the oligosaccharide processing enzyme mannosidase I. Transport between the ER and Golgi requires ATP and a cytosol fraction (a high speed supernatant of crude cell homogenates). Transport may occur in two biochemically distinct steps which correspond to the budding and fusion of transport vesicles. The goals of the proposal are: (1) To characterize the requirements for transport of G protein between compartments in the crude cell homogenate. (2) To purify, and characterize the donor ER, and acceptor cis Golgi compartments from crude cell homogenates which are active in transfer of protein in vitro. (3) To purify the soluble cytoplasmic components which are required for transport of protein, and characterize their possible role in vitro in the budding and fusion of carrier vesicles. (4) To define the morphological basis for the events occurring during transport in vitro using electron microscopy (EM), and EM immunocytochemistry. Movement of proteins between cellular organelles must require both common transport components, and specific recognition signals. An integrated biochemical and morphological approach using a experimentally versatile model system will provide a foundation to directly relate the events observed in vitro to those in vivo. Many medically important diseases result from defects in intracellular transport including lysosomal storage diseases, familial hypercholesterolemia, and cystic fibrosis. Considering the integral role of the secretory pathway in synthesis and maintenance of cell surface determinants, it is important to understand the initial stages of membrane biogenesis in regulation of cell growth and differentiation in order to achieve an understanding of the events leading to loss of growth control during oncogenesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
7R01GM033301-06
Application #
3282852
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1988-09-15
Project End
1992-03-31
Budget Start
1988-09-15
Budget End
1989-03-31
Support Year
6
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
San Diego
State
CA
Country
United States
Zip Code
92037
Rauniyar, Navin; Subramanian, Kanagaraj; Lavallée-Adam, Mathieu et al. (2015) Quantitative Proteomics of Human Fibroblasts with I1061T Mutation in Niemann-Pick C1 (NPC1) Protein Provides Insights into the Disease Pathogenesis. Mol Cell Proteomics 14:1734-49
Roth, Daniela Martino; Hutt, Darren M; Tong, Jiansong et al. (2014) Modulation of the maladaptive stress response to manage diseases of protein folding. PLoS Biol 12:e1001998
Hutt, Darren M; Balch, William E (2013) Expanding proteostasis by membrane trafficking networks. Cold Spring Harb Perspect Med 3:1-21
Powers, Evan T; Balch, William E (2013) Diversity in the origins of proteostasis networks--a driver for protein function in evolution. Nat Rev Mol Cell Biol 14:237-48
Pottekat, Anita; Becker, Scott; Spencer, Kathryn R et al. (2013) Insulin biosynthetic interaction network component, TMEM24, facilitates insulin reserve pool release. Cell Rep 4:921-30
Hutt, Darren M; Balch, William E (2013) Expanding proteostasis by membrane trafficking networks. Cold Spring Harb Perspect Biol 5:
Powers, Evan T; Balch, William E (2013) Diversity in the origins of proteostasis networks--a driver for protein function in evolution. Nat Rev Mol Cell Biol 14:237-48
Bouchecareilh, M; Balch, W E (2012) Proteostasis, an emerging therapeutic paradigm for managing inflammatory airway stress disease. Curr Mol Med 12:815-26
Bouchecareilh, Marion; Hutt, Darren M; Szajner, Patricia et al. (2012) Histone deacetylase inhibitor (HDACi) suberoylanilide hydroxamic acid (SAHA)-mediated correction of ýý1-antitrypsin deficiency. J Biol Chem 287:38265-78
Peters, Kathryn W; Okiyoneda, Tsukasa; Balch, William E et al. (2011) CFTR Folding Consortium: methods available for studies of CFTR folding and correction. Methods Mol Biol 742:335-53

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