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首页> 外文期刊>Biochemistry >Molecular weight determination of lipoprotein(a) (Lp(a)) in solutions containing either NaBr or D2O: relevance to the number of apolipoprotein(a) subunits in Lp(a).
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Molecular weight determination of lipoprotein(a) (Lp(a)) in solutions containing either NaBr or D2O: relevance to the number of apolipoprotein(a) subunits in Lp(a).

机译:含有NaBr或D2O的溶液中脂蛋白(a)(Lp(a))的分子量测定:与Lp(a)中载脂蛋白(a)亚基的数量有关。

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Molecular weight determination of low-density lipoprotein (LDL) is usually performed in solutions containing high concentrations of salt (up to 13.4 M NaBr) by sedimentation velocity and diffusion experiments, because it does not preferentially bind salt or water. Considering that lipoprotein(a) [Lp(a)] is structurally similar to LDL, differing only by the presence of Apo(a), the molecular weight, M, of Lp(a) has also been measured in solutions containing high concentrations of NaBr. We questioned the suitability of this practice by comparing the apparent molecular weight, Mapp, and partial volume, phi', of Lp(a) determined by sedimentation and flotation equilibrium in a three-component system containing NaBr with the analogous parameters, M and partial specific volume, v, determined in a two-component system containing D2O. LDL served as a control. In agreement with previous findings obtained with different methods, our results indicate no significant differences in M and v of four different LDL samples and apparently no significant preferential binding of solvent components. In contrast, values of Mapp and phi' of Lp(a) evaluated in NaBr are significantly greater than M and v. Preferential binding of solvent components appeared to be a function of Apo(a) mass or the number of kringle IV domains, as expressed by increasing percentage differences between the two sets of parameters, ranging from 4 to 13% in M and 0.2 to 0.5% in v of Lp(a) species having Apo(a) with 15-27 kringle IV domains. Furthermore, our results indicate that the variable Apo(a) kringle IV domains are more involved in this process than the constant domain of Apo(a). These findings indicate that the Lp(a) molecular weight should be determined in D2O and that high concentrations of NaBr should be avoided as their use would lead to overestimated molecular weights and partial specific volumes. Application of this method to the question of how much Apo(a) is released upon the reduction of Lp(a) led to the conclusion that Lp(a) contains only one Apo(a) molecule.
机译:低密度脂蛋白(LDL)的分子量测定通常是通过沉降速度和扩散实验在含有高浓度盐(至多13.4 M NaBr)的溶液中进行的,因为它不优先结合盐或水。考虑到脂蛋白(a)[Lp(a)]在结构上与LDL类似,仅区别在于Apo(a)的存在,因此在含有高浓度Lpo(a)的溶液中也测量了Lp(a)的分子量M。 NaBr。我们通过比较由LBr(a)的表观分子量分子量Mapp和部分体积phi'(通过沉淀和浮选平衡确定)在含NaBr的三组分系统中与类似参数M和部分部分相比较,对这种做法的适用性提出了质疑。在包含D2O的两组分系统中确定的比体积v。 LDL作为控件。与使用不同方法获得的先前发现相符,我们的结果表明四种不同LDL样品的M和v均无显着差异,并且显然没有明显的溶剂组分优先结合。相反,在NaBr中评估的Lp(a)的Mapp和phi'值显着大于M和v。溶剂组分的优先结合似乎是Apo(a)质量或kringle IV域数量的函数,因为表示是通过增加两组参数之间的百分比差异来表示的,其中M的范围为4至13%,v的具有Apo(a)且具有15-27个kringle IV域的Lp(a)物种的v为0.2至0.5%。此外,我们的结果表明,与恒定区Apo(a)相比,可变Apo(a)kringle IV结构域在此过程中的参与程度更高。这些发现表明,应在D2O中确定Lp(a)的分子量,应避免使用高浓度的NaBr,因为使用它们会导致分子量和部分比容过高。将这种方法应用于还原Lp(a)后释放多少Apo(a)的问题,得出的结论是Lp(a)仅包含一个Apo(a)分子。

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