Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity

To better understand the mechanism of lipid transfer protein (LTP) action and the effects of altered lipoprotein composition on its activity, we evaluated the dependence of LTP activity on the concentrations of cholesteryl ester (CE) and/or triglyceride (TG) in the phospholipid bilayer of substrate...

Full description

Bibliographic Details
Main Authors: RE Morton, JV Steinbrunner
Format: Article
Language:English
Published: Elsevier 1990-09-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520423405
id doaj-f7360b196eb3411888844fc7f6e31c9d
record_format Article
spelling doaj-f7360b196eb3411888844fc7f6e31c9d2021-04-25T04:22:14ZengElsevierJournal of Lipid Research0022-22751990-09-0131915591567Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activityRE Morton0JV Steinbrunner1Department of Vascular Cell Biology and Atherosclerosis Research, Cleveland Clinic Foundation, OH 44195.Department of Vascular Cell Biology and Atherosclerosis Research, Cleveland Clinic Foundation, OH 44195.To better understand the mechanism of lipid transfer protein (LTP) action and the effects of altered lipoprotein composition on its activity, we evaluated the dependence of LTP activity on the concentrations of cholesteryl ester (CE) and/or triglyceride (TG) in the phospholipid bilayer of substrate particles. Phosphatidylcholine (PC)-cholesterol liposomes containing up to 2 mole% TG and/or CE were prepared by cholate dialysis and used as either the donor of lipids to, or the acceptor of lipids from, low density lipoproteins (LDL). CE or TG transfer from liposomes of varying neutral lipid content to LDL showed saturation kinetics with an apparent Km of less than or equal to 0.2 mole%. Throughout this concentration-dependent response. PC transfer, which depended on the same LTP-donor particle binding interactions as those required for neutral lipid transfer, was essentially unchanged. Lipid transfer in the reverse direction (from LDL to liposomes of varying neutral lipid content) followed the same kinetics showing that transfer between the two particles is tightly coupled and bidirectional. When liposomes contained both TG and CE, these lipids competed for transfer in a manner analogous to that previously noted with lipoprotein substrates. In conclusion, CE and TG transfer activities are determined by the concentration of these lipids in the phospholipid surface of donor and acceptor particles. At low TG and CE concentrations, LTP bound to the liposome surface as indicated by PC transfer, but only a portion of these interactions actually facilitated a neutral lipid transfer event. Thus, the overall rate of neutral lipid transfer, and the competition between TG and CE for transfer, depend on the concentrations of these lipids in the phospholipid layer.http://www.sciencedirect.com/science/article/pii/S0022227520423405
collection DOAJ
language English
format Article
sources DOAJ
author RE Morton
JV Steinbrunner
spellingShingle RE Morton
JV Steinbrunner
Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity
Journal of Lipid Research
author_facet RE Morton
JV Steinbrunner
author_sort RE Morton
title Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity
title_short Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity
title_full Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity
title_fullStr Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity
title_full_unstemmed Concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity
title_sort concentration of neutral lipids in the phospholipid surface of substrate particles determines lipid transfer protein activity
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1990-09-01
description To better understand the mechanism of lipid transfer protein (LTP) action and the effects of altered lipoprotein composition on its activity, we evaluated the dependence of LTP activity on the concentrations of cholesteryl ester (CE) and/or triglyceride (TG) in the phospholipid bilayer of substrate particles. Phosphatidylcholine (PC)-cholesterol liposomes containing up to 2 mole% TG and/or CE were prepared by cholate dialysis and used as either the donor of lipids to, or the acceptor of lipids from, low density lipoproteins (LDL). CE or TG transfer from liposomes of varying neutral lipid content to LDL showed saturation kinetics with an apparent Km of less than or equal to 0.2 mole%. Throughout this concentration-dependent response. PC transfer, which depended on the same LTP-donor particle binding interactions as those required for neutral lipid transfer, was essentially unchanged. Lipid transfer in the reverse direction (from LDL to liposomes of varying neutral lipid content) followed the same kinetics showing that transfer between the two particles is tightly coupled and bidirectional. When liposomes contained both TG and CE, these lipids competed for transfer in a manner analogous to that previously noted with lipoprotein substrates. In conclusion, CE and TG transfer activities are determined by the concentration of these lipids in the phospholipid surface of donor and acceptor particles. At low TG and CE concentrations, LTP bound to the liposome surface as indicated by PC transfer, but only a portion of these interactions actually facilitated a neutral lipid transfer event. Thus, the overall rate of neutral lipid transfer, and the competition between TG and CE for transfer, depend on the concentrations of these lipids in the phospholipid layer.
url http://www.sciencedirect.com/science/article/pii/S0022227520423405
work_keys_str_mv AT remorton concentrationofneutrallipidsinthephospholipidsurfaceofsubstrateparticlesdetermineslipidtransferproteinactivity
AT jvsteinbrunner concentrationofneutrallipidsinthephospholipidsurfaceofsubstrateparticlesdetermineslipidtransferproteinactivity
_version_ 1721510286772404224