Jonas A
Biochim Biophys Acta. 1975 Jun 26;393(2):460-70. doi: 10.1016/0005-2795(75)90074-4.
The delipidated protein component of bovine serum high density lipoprotein was fractionated by gel filtration on a Sephadex G-150 column (equilibrated with buffer containing 6 M urea) into three fractions: I, II and III. Fractions I and II together constitute 88% of all the protein weight of bovine high density lipoprotein, whereas fraction III accounts for the remaining 12%. Analysis of the fractions by sodium dodecyl sulfate-polyacrylamide electrophoresis reveals that fraction I consists mostly of aggregated forms of fraction II and some higher molecular weight species, probably irreversible aggregates of fraction II. The irreversible aggregates are apparently formed during the delipidation procedure or upon aging of the lipoprotein. The major protein component of the high density bovine lipoprotein is found in fraction II; it has a molecular weight of 27 000 plus or minus 1500 and appears to be homogeneous by several physicochemical criteria. The amino acid composition of fractions I and II are essentially identical; their spectral properties, including absorption, fluorescence, and circular dichroism spectra, are similar; however, fraction I appears to contain traces of oxidized lipid and more secondary alpha-helical organization than fraction II. By comparison with the intact lipoprotein, which contains about 65% of alpha-helical structure, fractions I and II have diminished alpha-helical organization, 55% and 43%, respectively. Fraction III, on sodium dodecyl sulfate-polyacrylamide electrophoresis, separates into two protein bands of equivalent intensity, having molecular weights around 13 000 and 11 000. Fraction III is markedly distinct from the other two, in amino acid composition and spectral properties, especially in its red-shifted fluorescence and very low content of alpha-helical structure. The protein composition of bovine serum high density lipoprotein is compared with recently published results for high density lipoprotein apoproteins of man, chimpanzee, rhesus monkey, pig and rat. Similarities and differences are discussed in terms of possible evolutionary and functional factors.
牛血清高密度脂蛋白的脱脂蛋白成分通过在葡聚糖G - 150柱(用含6M尿素的缓冲液平衡)上进行凝胶过滤,被分离成三个组分:I、II和III。组分I和II一起占牛高密度脂蛋白所有蛋白质重量的88%,而组分III占其余的12%。通过十二烷基硫酸钠 - 聚丙烯酰胺电泳对这些组分进行分析表明,组分I主要由组分II的聚集形式和一些较高分子量的物质组成,可能是组分II的不可逆聚集体。这些不可逆聚集体显然是在脱脂过程中或脂蛋白老化时形成的。高密度牛脂蛋白的主要蛋白质成分存在于组分II中;其分子量为27000±1500,并且通过几种物理化学标准来看似乎是均一的。组分I和II的氨基酸组成基本相同;它们的光谱特性,包括吸收光谱、荧光光谱和圆二色光谱,是相似的;然而,组分I似乎含有痕量的氧化脂质,并且比组分II具有更多的二级α - 螺旋结构。与含有约65%α - 螺旋结构的完整脂蛋白相比,组分I和II的α - 螺旋结构减少,分别为55%和43%。在十二烷基硫酸钠 - 聚丙烯酰胺电泳中,组分III分离成两条强度相当的蛋白带,分子量约为13000和11000。组分III在氨基酸组成和光谱特性上与其他两个组分明显不同,特别是在其红移荧光和极低的α - 螺旋结构含量方面。将牛血清高密度脂蛋白的蛋白质组成与最近发表的关于人、黑猩猩、恒河猴、猪和大鼠的高密度脂蛋白载脂蛋白的结果进行了比较。从可能的进化和功能因素方面讨论了异同点。