Comparison of ultracentrifugation and gel filtration for the isolation of bovine lipoproteins

色谱法 化学 大小排阻色谱法 洗脱 超离心机 脂蛋白 电泳 分馏 琼脂糖 低密度脂蛋白 生物化学 胆固醇
作者
R.R. Grummer,C.L. Davis,H.M. Hegarty
出处
期刊:Lipids [Wiley]
卷期号:18 (11): 795-802 被引量:26
标识
DOI:10.1007/bf02534638
摘要

Abstract Lipoproteins from the plasma of three nonlactating Holstein cows were isolated using either preparative ultracentrifugation or gel filtration chromatography. Lipoprotein classes obtained by ultracentrifugation were very low density plus chylomicra, <1.006 g/ml; low density, 1.007–1.039 g/ml; high density 1 , 1.040–1.063 g/ml; and high density, 1.064–1.22 g/ml. These lipoprotein classes were individually applied to an agarose gel column to determine at what volume they eluted in comparison to lipoproteins that were separated after applying total bovine lipoproteins to the column. Three major peaks corresponding to very low density lipoproteins plus chylomicra, low density, and high density lipoproteins resulted after gel filtration of total lipoproteins. Very low density lipoproteins plus chylomicra, obtained by ultracentrifugation, eluted as a single peak, as did low density and high density lipoproteins. However, high density 1 lipoproteins eluted as two peaks. The first peak eluted at the same volume as low density lipoproteins, and the second peak eluted at a volume similar to that of the ascending slope of the high density lipoprotein peak. Results from disc polyacrylamide gel electrophoresis, immunoelectrophoresis and double immunodiffusion of lipoprotein fractions, and SDS polyacrylamide gel electrophoresis of their apoproteins, similarly indicated that the lipoproteins present in the 1.040–1.063 g/ml density interval are a mixture of low and high density lipoproteins rather than a unique class of lipoproteins.
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