The long-term goal of this research is to understand how the distribution of free and esterified cholesterol is regulated, both among tissue and among intracellular pools. This project is concerned with specific regulatory aspects of the overall process. Primary focus is on the regulation of the interfacial reaction. CHOLESTERYL ESTER + WATER EQUILIBRIUM WITH FATTY ACID + CHOLESTEROL as catalyzed by mammalian cholesterol esterases. Related to this is the regulation of the spontaneous transport of lipid substrate and products to and away from the reaction site. In this regard, the partitioning of free cholesterol into the aqueous phase and the movement of cholesterol and cholesteryl ester across bilayers will be addressed. An important characteristic of both the hydrolysis reaction and the transport reactions is that they are interfacial. Hence, the major experimental emphasis is on the role of lipid- lipid and lipid-protein interactions in surface phases in the regulation of these processes. Specifically, rates and extents of enzyme adsorption to and substrate hydrolysis in surface phases at the argon-buffer interface will be measured. The enzymes to be used are pancreatic carboxylester lipase, lysosomal cholesterol esterase and hormone sensitive cholesterol esterase. Emphasis is on determining how these enzymes are regulated by specific lipid- lipid interactions. From the results obtained apparent enzyme specificity can be separated into physical and chemical specificities. Studies of the regulation of the spontaneous transfer of cholesterol and cholesteryl ester across bilayers will reveal under what conditions cholesterol esterases may facilitate cholesterol movement across bilayers. The achievement of these aims will greatly increase our understanding of the regulation of the distribution of cholesterol between chemical forms and physical pools in vivo.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL017371-16
Application #
3335332
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1978-01-01
Project End
1993-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
16
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Other Domestic Higher Education
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Liang, Y; Medhekar, R; Brockman, H L et al. (2000) Importance of arginines 63 and 423 in modulating the bile salt-dependent and bile salt-independent hydrolytic activities of rat carboxyl ester lipase. J Biol Chem 275:24040-6
Li, X M; Smaby, J M; Momsen, M M et al. (2000) Sphingomyelin interfacial behavior: the impact of changing acyl chain composition. Biophys J 78:1921-31
Brockman, H (1999) Lipid monolayers: why use half a membrane to characterize protein-membrane interactions? Curr Opin Struct Biol 9:438-43
Ali, S; Smaby, J M; Momsen, M M et al. (1998) Acyl chain-length asymmetry alters the interfacial elastic interactions of phosphatidylcholines. Biophys J 74:338-48
Smaby, J M; Momsen, M M; Brockman, H L et al. (1997) Phosphatidylcholine acyl unsaturation modulates the decrease in interfacial elasticity induced by cholesterol. Biophys J 73:1492-505
Momsen, W E; Brockman, H L (1997) Recovery of monomolecular films in studies of lipolysis. Methods Enzymol 286:292-305
Kennedy, M T; Brockman, H; Rusnak, F (1997) Determinants of calcineurin binding to model membranes. Biochemistry 36:13579-85
Smaby, J M; Momsen, M; Kulkarni, V S et al. (1996) Cholesterol-induced interfacial area condensations of galactosylceramides and sphingomyelins with identical acyl chains. Biochemistry 35:5696-704
Myers-Payne, S C; Hui, D Y; Brockman, H L et al. (1995) Cholesterol esterase: a cholesterol transfer protein. Biochemistry 34:3942-7
Smaby, J M; Muderhwa, J M; Brockman, H L (1994) Is lateral phase separation required for fatty acid to stimulate lipases in a phosphatidylcholine interface? Biochemistry 33:1915-22

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