Phospholipids are a diverse class of amphipathic molecules present in all biologicial membranes. Because of the experimental difficulties encountered in working with membrane components, relatively little is known about the enzymatic and genetic control of phospholipid metabolism or about the role of individual phospholipid species in membrane function. A greater understanding of this fundamental aspect of membrane biochemistry would be desirable, since phospholipids play an important role in many disease processes, including hyperlipoproteinemias, diabetes, and certain inborn errors of metabolism. The isolation and characterization of animal cell mutants lacking specific phospholipid molecules are the major goals of this project. The physiology of such mutants is expected to shed light on phospholipid regulation and function. In the long run these mutants should facilitate the isolation of the genes that code for the enzymes involved in the synthesis and assembly of higher eucaryotic membrane lipids. It is estimated that there must be several hundred of such genes in an animal cell, but only a few mutants have been isolated so far. In the coming grant period, three major projects will be emphasized. 1) The laboratory will develop schemes for the isolation of animal cell mutants deficient in the enzymes of phosphatidylinositol synthesis, phosphorylation, and turnover. 2) The biochemistry and genetics of animal cell mutants deficient in the biosynthesis of plasmalogens will be studied. During the last grant period a collection of Chinese hamster ovary cell mutants deficient in the peroxisomal dihydroxyacetone phosphate acyltransferase was isolated, an enzyme that is also missing in Zellweger's syndrome. 3) The interaction of Escherichia coli lipid A molecules with membranes of animal cells will be characterized. Recent studies from the PI's laboratory have led to the elucidation of the biosynthesis of lipid A in E. coli. The resulting new enzymology provides a unique opportunity to make labeled probes for studying the mechanisms by which lipid A molecules trigger responses in animal cells, such as macrophage activation or mitogenesis. The above studies will advance fundamental understanding of the role of lipid molecules in cell membranes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK021722-09
Application #
3227095
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1978-07-01
Project End
1991-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
9
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Earth Sciences/Resources
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Hofer, M; Hampton, R Y; Raetz, C R et al. (1991) Aggregation behavior of lipid IVA in aqueous solutions at physiological pH. 1: Simple buffer solutions. Chem Phys Lipids 59:167-81
Morand, O H; Allen, L A; Zoeller, R A et al. (1990) A rapid selection for animal cell mutants with defective peroxisomes. Biochim Biophys Acta 1034:132-41
Raetz, C R (1990) Biochemistry of endotoxins. Annu Rev Biochem 59:129-70
Golenbock, D T; Hampton, R Y; Raetz, C R et al. (1990) Human phagocytes have multiple lipid A-binding sites. Infect Immun 58:4069-75
Zoeller, R A; Allen, L A; Santos, M J et al. (1989) Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome. J Biol Chem 264:21872-8
Allen, L A; Morand, O H; Raetz, C R (1989) Cytoplasmic requirement for peroxisome biogenesis in Chinese hamster ovary cells. Proc Natl Acad Sci U S A 86:7012-6
Morand, O H; Zoeller, R A; Raetz, C R (1988) Disappearance of plasmalogens from membranes of animal cells subjected to photosensitized oxidation. J Biol Chem 263:11597-606
Naleway, J J; Raetz, C R; Anderson, L (1988) A convenient synthesis of 4-amino-4-deoxy-L-arabinose and its reduction product, 1,4-dideoxy-1,4-imino-L-arabinitol. Carbohydr Res 179:199-209
Sibley, C H; Terry, A; Raetz, C R (1988) Induction of kappa light chain synthesis in 70Z/3 B lymphoma cells by chemically defined lipid A precursors. J Biol Chem 263:5098-103
Hampton, R Y; Golenbock, D T; Raetz, C R (1988) Lipid A binding sites in membranes of macrophage tumor cells. J Biol Chem 263:14802-7

Showing the most recent 10 out of 13 publications