Swaney J B, Gidez L I
J Lipid Res. 1977 Jan;18(1):69-76.
The low molecular weight proteins of rat apo HDL and apo VLDL have been isolated and analyzed by the technique of isoelectric focusing. Sephadex fractions from apo HDL (HS-3) and apo VLDL (VS-3) that contain these proteins reveal three major bands with apparent isoelectric points of pH 4.50, 4.67, and 4.74, as well as three minor bands at pH 4.43, 4.57, and 4.61. In addition, apo HDL has a major band at pI of 4.83. DEAE-Cellulose chromatography was used to prepare purified fractions of these components that were characterized by N-terminal analyses and molecular weight determinantions by SDS gel electrophoresis. The major low molecular weight components of apo HDL were focused on a slab gel and the bands were identified as A-II (pI 4.83), C-II (pI 4.74), C-III-0 (pI 4.67), and C-III-3 (pI 4.50). Neuraminidase treatment of apo HDL, followed by isoelectric focusing, suggested that the other bands, which have not previously been reported, may be additional forms of the C-III protein, differing only in their content of sialic acid.
已采用等电聚焦技术分离并分析了大鼠载脂蛋白高密度脂蛋白(apo HDL)和载脂蛋白极低密度脂蛋白(apo VLDL)的低分子量蛋白质。来自含有这些蛋白质的apo HDL(HS - 3)和apo VLDL(VS - 3)的葡聚糖凝胶分离级分显示出三条主要条带,其表观等电点分别为pH 4.50、4.67和4.74,以及在pH 4.43、4.57和4.61处的三条次要条带。此外,apo HDL在pI为4.83处有一条主要条带。使用二乙氨基乙基纤维素(DEAE - Cellulose)色谱法制备这些组分的纯化级分,并通过N端分析和十二烷基硫酸钠(SDS)凝胶电泳进行分子量测定来对其进行表征。将apo HDL的主要低分子量组分聚焦在平板凝胶上,这些条带被鉴定为A - II(pI 4.83)、C - II(pI 4.74)、C - III - 0(pI 4.67)和C - III - 3(pI 4.50)。对apo HDL进行神经氨酸酶处理,然后进行等电聚焦,结果表明,此前未报道过的其他条带可能是C - III蛋白的其他形式,只是它们的唾液酸含量不同。