A low temperature flotation method to rapidly isolate lipoproteins from plasma
To minimize oxidative modification, a low temperature, sequential flotation method was developed to isolate plasma lipoproteins in 18 h using a benchtop ultracentrifuge. The protein distributions were characterized using agarose and SDS-polyacrylamide gel electrophoresis, and an SDS-Lowry protein as...
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doaj-e6fbef60fbb141bb8949278055abee0d2021-04-26T05:45:46ZengElsevierJournal of Lipid Research0022-22751998-08-0139816961704A low temperature flotation method to rapidly isolate lipoproteins from plasmaH. Tong0H.R. Knapp1M. VanRollins2Division of Clinical Pharmacology, Department of Internal Medicine, College of Medicine, The University of Iowa, Iowa City, IA 52242Division of Clinical Pharmacology, Department of Internal Medicine, College of Medicine, The University of Iowa, Iowa City, IA 52242To whom correspondence should be addressed.; Division of Clinical Pharmacology, Department of Internal Medicine, College of Medicine, The University of Iowa, Iowa City, IA 52242To minimize oxidative modification, a low temperature, sequential flotation method was developed to isolate plasma lipoproteins in 18 h using a benchtop ultracentrifuge. The protein distributions were characterized using agarose and SDS-polyacrylamide gel electrophoresis, and an SDS-Lowry protein assay. The lipid distributions were assessed using a gas chromatography–mass spectrometric assay for cholesterol and an enzymatic assay for triglycerides. To validate the rapid flotation method, lipoproteins were also isolated from the same plasma samples using a modified Havel et al. flotation method (J. Clin. Invest. 34: 1345–1353, 1955). The same lipoproteins and apolipoproteins were present in fractions of comparable density, and the summed recoveries of protein, cholesterol, and triglyceride were also identical for the Havel et al. and rapid flotation procedures. Likewise, the amount of cholesterol and triglyceride in corresponding very low, intermediate, and low density lipoprotein (VLDL/IDL and LDL) fractions was the same for the two flotation procedures. The triglyceride and cholesterol levels in high density lipoprotein (HDL) isolated by rapid flotations, however, were 9–12% higher than in the HDL as isolated by Havel et al. Because a 9–12% increase in the HDL fraction reflects only 1–4% of the total triglyceride and cholesterol in plasma, we conclude that, while maintained at 4°C, lipoproteins were quantitatively isolated from human plasma in 1 day.—Tong, H., H. R. Knapp, and M. VanRollins. A low temperature flotation method to rapidly isolate lipoproteins from plasma.http://www.sciencedirect.com/science/article/pii/S0022227520322008ultracentrifugationhuman plasmavery low density lipoproteinslow density lipoproteinshigh density lipoproteinsmass spectrometry |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
H. Tong H.R. Knapp M. VanRollins |
spellingShingle |
H. Tong H.R. Knapp M. VanRollins A low temperature flotation method to rapidly isolate lipoproteins from plasma Journal of Lipid Research ultracentrifugation human plasma very low density lipoproteins low density lipoproteins high density lipoproteins mass spectrometry |
author_facet |
H. Tong H.R. Knapp M. VanRollins |
author_sort |
H. Tong |
title |
A low temperature flotation method to rapidly isolate lipoproteins from plasma |
title_short |
A low temperature flotation method to rapidly isolate lipoproteins from plasma |
title_full |
A low temperature flotation method to rapidly isolate lipoproteins from plasma |
title_fullStr |
A low temperature flotation method to rapidly isolate lipoproteins from plasma |
title_full_unstemmed |
A low temperature flotation method to rapidly isolate lipoproteins from plasma |
title_sort |
low temperature flotation method to rapidly isolate lipoproteins from plasma |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
1998-08-01 |
description |
To minimize oxidative modification, a low temperature, sequential flotation method was developed to isolate plasma lipoproteins in 18 h using a benchtop ultracentrifuge. The protein distributions were characterized using agarose and SDS-polyacrylamide gel electrophoresis, and an SDS-Lowry protein assay. The lipid distributions were assessed using a gas chromatography–mass spectrometric assay for cholesterol and an enzymatic assay for triglycerides. To validate the rapid flotation method, lipoproteins were also isolated from the same plasma samples using a modified Havel et al. flotation method (J. Clin. Invest. 34: 1345–1353, 1955). The same lipoproteins and apolipoproteins were present in fractions of comparable density, and the summed recoveries of protein, cholesterol, and triglyceride were also identical for the Havel et al. and rapid flotation procedures. Likewise, the amount of cholesterol and triglyceride in corresponding very low, intermediate, and low density lipoprotein (VLDL/IDL and LDL) fractions was the same for the two flotation procedures. The triglyceride and cholesterol levels in high density lipoprotein (HDL) isolated by rapid flotations, however, were 9–12% higher than in the HDL as isolated by Havel et al. Because a 9–12% increase in the HDL fraction reflects only 1–4% of the total triglyceride and cholesterol in plasma, we conclude that, while maintained at 4°C, lipoproteins were quantitatively isolated from human plasma in 1 day.—Tong, H., H. R. Knapp, and M. VanRollins. A low temperature flotation method to rapidly isolate lipoproteins from plasma. |
topic |
ultracentrifugation human plasma very low density lipoproteins low density lipoproteins high density lipoproteins mass spectrometry |
url |
http://www.sciencedirect.com/science/article/pii/S0022227520322008 |
work_keys_str_mv |
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