A subscription to JoVE is required to view this content. Sign in or start your free trial.
Several methods have been used for analyzing plasma lipoproteins; however, ultracentrifugation is still one of the most popular and reliable methods. Here, we describe a method regarding how to isolate lipoproteins from plasma using sequential density ultracentrifugation and how to analyze the apolipoproteins for both diagnostic and research purposes.
Analysis of plasma lipoproteins and apolipoproteins is an essential part for the diagnosis of dyslipidemia and studies of lipid metabolism and atherosclerosis. Although there are several methods for analyzing plasma lipoproteins, ultracentrifugation is still one of the most popular and reliable methods. Because of its intact separation procedure, the lipoprotein fractions isolated by this method can be used for analysis of lipoproteins, apolipoproteins, proteomes, and functional study of lipoproteins with cultured cells in vitro. Here, we provide a detailed protocol to isolate seven lipoprotein fractions including VLDL (d<1.006 g/mL), IDL (d=1.02 g/mL), LDLs (d=1.04 and 1.06 g/mL), HDLs (d=1.08, 1.10, and 1.21 g/mL) from rabbit plasma using sequential floating ultracentrifugation. In addition, we introduce the readers how to analyze apolipoproteins such as apoA-I, apoB, and apoE by SDS-PAGE and Western blotting and show representative results of lipoprotein and apolipoprotein profiles using hyperlipidemic rabbit models. This method can become a standard protocol for both clinicians and basic scientists to analyze lipoprotein functions.
Dyslipidemia is the major risk factor of atherosclerotic disease in the world. High levels of low-density lipoproteins (LDLs) and low levels of high-density lipoproteins (HDLs) are closely associated with a high risk of coronary heart disease (CHD)1,2. In the clinical setting, both LDL-cholesterol (LDL-C) and HDL-cholesterol (HDL-C) are routinely measured using an automated analyzer in a clinical laboratory3,4. Despite this, it is essential to analyze lipoprotein profiles in details for the diagnosis of dyslipidemia and the study of lipid metabolism an....
All procedures for rabbit studies were performed with approval of University of Yamanashi Institutional Animal Care and Use Committee (Approved number: A28-39).
1. Plasma separation from rabbit blood
Using this protocol, we isolated rabbit lipoproteins using 1 mL of plasma and obtained seven density fractions. Isolated density fractions are enough for measuring lipids and apolipoproteins as described above for most research purposes. The same procedure can also be used for isolating plasma lipoproteins from human and other species. For small-sized animals such as mice, pooled plasma is required. Figure 3 shows lipoprotein profiles of wild-type (WT) rabbits fed either a normal standard (N.......
Hyperlipidemia is one of the most important risk factors of atherosclerotic disease. Thus, analysis of plasma lipoproteins is not only essential for diagnosis of dyslipidemia patients but also important for investigation of molecular mechanisms of lipoprotein metabolism and atherosclerosis. In this study, we described the protocol of isolation and analysis of plasma lipoproteins which can be applied in the laboratories where ultracentrifugation is available. Information obtained by this method is comprehensive and straig.......
This work was supported in part by a research grants from JSPS KAKENHI Grant Number JP 20K08858, the National Natural Science Foundation of China (No. 81941001 and 81770457), JSPS-CAS under the Japan-China Research Cooperative Program.
....Name | Company | Catalog Number | Comments |
22-gauge needle | Terumo | NN-2232S | For blood collection |
96-well microplate | greiner bio-one | 655101 | For lipids measurment |
Anti-apolipoprotein A-I antibody | LifeSpan BioSciences | LS-C314186 | For Western blottng, use 1:1,000 |
Anti-apolipoprotein B antibody | ROCKLAND | 600-101-111 | For Western blottng, use 1:1,000 |
Anti-apolipoprotein E antibody | Merck Millipore | AB947 | For Western blottng, use 1:1,000 |
CBB staining kit | FUJIFILM Wako Pure Chemical | 299-50101 | For apolipoprotein analysis |
Centrifuge | HITACHI | himac CF15RN | |
Closure | Spectrum | 132736 | For lipoprotein dialysis |
Dialysis tubing | FUJIFILM Wako Pure Chemical | 043-30921 | For lipoprotein dialysis, MWCO 14,000 |
Dry heat block | Major Science | MD-01N | For SDS-PAGE sample preparation |
ECL Western blotting detection reagents | GE Healthcare | RPN2209 | For Western blotting |
Electrophoresis Chamber | BIO-RAD | Mini-PROTEAN Tetra Cell | |
Ethylenediamine-N,N,N',N'-tetraacetic acid (EDTA) disodium salt dihydrate | FUJIFILM Wako Pure Chemical | 345-01865 | For anticoagulant (0.5 M), for dialysis (1 mM) |
Filter paper | ADVANTEC | 590 | For Western blotting |
Fixed angle ultracentrifuge rotor | BECKMAN COULTER | 357656 | TLA-120.2 |
Fixing solution | For SDS-PAGE (50% Methanol/ 10% Acetic acid) | ||
Immun-Blot PVDF menbrane | BIO-RAD | 1620177 | For Western blotting |
Lumino image analyzer | GE Healthcare | For Western blotting, ImageQuant LAS 4000 | |
Magnetic stirrer | ADVANTEC | SR-304 | For lipoprotein dialysis |
Microplate reader iMARK | BIO-RAD | For lipids measurment | |
Microtube | INA-OPTIKA | SC-0150 | |
Orbital agitator USBDbo | Stovall Life Science | ||
Peroxidase congugated anti goat IgG antibody | Jackson ImmunoResearch | 705-035-003 | For Western blotting, use 1:2,000 |
Peroxidase congugated anti mouse IgG antibody | Jackson ImmunoResearch | 715-035-150 | For Western blotting, use 1:2,000 |
Phospholipids assay kit | FUJIFILM Wako Pure Chemical | 433-36201 | For lipids measurment |
Polycarbonate ultracentrifuge Tubes | BECKMAN COULTER | 343778 | |
Potassium Bromide | FUJIFILM Wako Pure Chemical | 168-03475 | For density solution |
Power Supply | BIO-RAD | For SDD-PAGE and Western blotting, PowerPac 300, PowerPac HC | |
Protein standards Precidion Plus Protein Dual Xtra | BIO-RAD | 161-0377 | For SDS-PAGE and Western blotting |
Rabbit restrainer | Natsume Seisakusho | KN-318 | For blood collection |
Rotor | HITACHI | T15A43 | |
SDS-PAGE running buffer | 25 mM Tris/ 192 mM Glycine/ 0.1% SDS | ||
SDS-PAGE sample buffer (2x) | 0.1M Tris-HCl (pH 6.8)/ 4% SDS/ 20% glycerol/ 0.01% BPB/12% 2-merpaptoethanol | ||
SDS-polyacrylamide gel | 4-20% gradient polyacrylamide gel | ||
Skim milk powder | FUJIFILM Wako Pure Chemical | 190-12865 | For Western blotting blocking buffer (5% skim milk/ 0.1% Tween 20/ PBS) |
Total cholesterol assay kit | FUJIFILM Wako Pure Chemical | 439-17501 | For lipids measurment |
Triglyicerides assay kit | FUJIFILM Wako Pure Chemical | 432-40201 | For lipids measurment |
Tube slicer for thick-walled tube | BECKMAN COULTER | 347960 | For lipoprotein isolation |
Tween 20 | SIGMA-ALDRICH | P1379 | For Western blotting washing buffer (0.1% Tween 20/ PBS) |
Ultracentrifuge | BECKMAN COULTER | A95761 | Optima MAX-TL |
Western blotting wet transfer system | BIO-RAD | Mini Trans-Blot Cell |
This article has been published
Video Coming Soon
ABOUT JoVE
Copyright © 2024 MyJoVE Corporation. All rights reserved