Marcel Y L, Bergseth M, Nestruck A C
Biochim Biophys Acta. 1979 Apr 27;573(1):175-83. doi: 10.1016/0005-2760(79)90184-x.
The application of isoelectric focussing on a gel-stabilized layer for the separation of the Tris-urea-soluble apolipoproteins of very low density lipoproteins has been described. This method in one step, allows the separation of most apolipoproteins, which were then analyzed and characterized. Apolipoproteins CII and CI were isolated as single protein bands with apparent pI of 5.0 and 6.5, respectively. Apolipoprotein CII was biologically active and could activate lipoprotein lipase. Apolipoprotein CIII was separated into several protein bands with pI ranging from 4.7 to 5.1 as a function of their number of sialic acid residues. Apolipoprotein E was isolated and characterized into five polymorphic bands with pI of 5.7, 5.8, 5.9, 6.0, and 6.2, respectively.
已描述了等电聚焦在凝胶稳定层上用于分离极低密度脂蛋白的Tris-尿素可溶性载脂蛋白的应用。该方法一步就能分离出大多数载脂蛋白,然后对其进行分析和表征。载脂蛋白CII和CI分别作为表观pI为5.0和6.5的单一蛋白条带被分离出来。载脂蛋白CII具有生物活性,能够激活脂蛋白脂肪酶。载脂蛋白CIII根据其唾液酸残基数量被分离为几个pI范围为4.7至5.1的蛋白条带。载脂蛋白E被分离并表征为五个多态性条带,其pI分别为5.7、5.8、5.9、6.0和6.2。