Isolation of plasma lipoproteins

Lipoproteins were isolated from plasma of man, dog, rabbit, rat, and chicken by ultracentrifugation in continuous density gradients using the B14 titanium and B15 titanium zonal rotors. Both the VLDL and the LDL of human plasma were separated easily from the HDL and from the other more plentiful plasma proteins by centrifugation for only 1 or 2 hr in the B14 or B15 rotor, respectively. Satisfactory separation of the HDL from the more dense plasma proteins was not achieved with these rotors. The human LDL achieved isopycnic equilibrium (d 1.04) on prolonged periods (> 24 hr) of centrifugation in a sucrose-KBr density gradient. The pattern of distribution of cholesterol and phospholipid throughout the density gradient coincided with the pattern of distribution of the lipoprotein-protein measured spectrophotometrically or chemically. The concentration of cholesterol and phospholipid in the lipoproteins isolated by zonal ultracentrifugation agreed with analyses reported for lipoproteins isolated by sequential centrifugation in solutions of increasing density. The lipoproteins isolated by zonal ultracentrifugation were characterized further by their electrophoretic behavior. The fractions which were identified as the LDL (d 1.04-1.05) from all species migrated on paper as a &globulin; the LDL from plasma of dogs contained an additional component which has been designated as an a2-globulin. The fractions which were identified as the HDL from all species migrated as an aL-globulin. Reaction of human LDL with either rabbit antihuman 0lipoprotein or rabbit antihuman serum resulted in a single immunodiffusion band. The Sf,,.o63 of the human LDL was calculated to be 6.0. When plasma from humans or rabbits was Abbreviations: VLDL, very low density lipoprotein, d < 1.006; LDL, low density lipoprotein, d 1.006-1.063; HDL, high density lipoprotein, d 1.063-1.210; d, density; C, cholesterol; PL, phospholipid; EDTA, ethylenediamine-tetraacetic acid. * Part of this work was completed during the tenure of a Postdoctoral Fellowship from the National Institutes of Health, No. 2 $ This work was done, in part, during the tenure of an EstabF 2AM-24232. lished Investigatorship of the American Heart Association. centrifuged in the B15 rotor, the HDL was not visible as a distinct peak and was not separable from the bulk of the more dense plasma proteins; when plasma from dogs or chickens was centrifuged under identical conditions, the HDL was clearly detectable. Even though the mean density of the HDL from dogs or chickens was not different from that of man or rabbits, the visibility of this lipoprotein in dogs and chickens was probably due to its high concentration in the plasma of these species. When plasma from the rat was centrifuged under similar conditions, the HDL was also clearly in evidence. Although rat plasma contained a relatively small concentration of HDL, the lipoprotein had a lower mean density than did the HDL of the other species and was therefore more easily separable from the dense plasma proteins. The procedure of zonal ultracentrifugation for the isolation of lipoproteins by flotation is simultaneously preparative and analytical and should find useful application in the investigation of the soluble lipoproteins from plasma and tissues. SUPPLEMENTARY