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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Miniaturization of asymmetrical flow field-flow fractionation and application to studies on lipoprotein aggregation and fusion
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Miniaturization of asymmetrical flow field-flow fractionation and application to studies on lipoprotein aggregation and fusion

机译:非对称流场流分离的小型化及其在脂蛋白聚集与融合研究中的应用

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Asymmetrical flow field-flow fractionation (AsFIFFF), a technique that provides direct measurement of particle size and diffusion coefficient, is converted into miniaturized scale. In comparison with conventional AsFIFFF, the separation of proteins in miniaturized AsFIFFF is achieved within shorter time periods, with smaller sample amounts, and with lower mobile phase consumption. Minimization of the overloading and optimization of the separation efficiency are prerequisites to good results. Miniaturized AsFIFFF is applied to the measurement of particle sizes of high-density lipoprotein (HDL). low-density lipoprotein (LDL), and very low-density lipoprotein (VLDL). The average hydrodynamic diameters at pH 7.4 in 8.5 mM phosphate buffer containing I mM EDTA and 150 mM NaCl are 8.6 +/- 0.5, 11.2 +/- 10.2, 22.1 +/- 0.7. and 48.9 +/- 7.5 nm for subgroups HDL3. HDL2. LDL, and VLDL, respectively. In addition. the effect of different factors on the aggregation and fusion of LDL particles is studied. LDL particle sizes are unaffected by the addition of up to 300 mM NaCl and by an increase of the carrier solution pH from 3.2 to 7.4. but treatment of LDL with alpha-chymotrypsin, sphingomyelinase, or copper sulfate leads to the formation of aggregated and fused LDL particles. (c) 2006 Elsevier Inc. All rights reserved.
机译:非对称流场流分馏(AsFIFFF)是一种可直接测量粒度和扩散系数的技术,现已转换为小型化规模。与传统的AsFIFFF相比,微型化的AsFIFFF中的蛋白质分离可在更短的时间内,更少的样品量和更低的流动相消耗中实现。最小化过载和优化分离效率是获得良好结果的前提。小型化的AsFIFFF用于测量高密度脂蛋白(HDL)的粒径。低密度脂蛋白(LDL)和极低密度脂蛋白(VLDL)。在含有1 mM EDTA和150 mM NaCl的8.5 mM磷酸盐缓冲液中,pH 7.4时的平均流体动力学直径为8.6 +/- 0.5、11.2 +/- 10.2、22.1 +/- 0.7。 HDL3子组为48.9 +/- 7.5 nm。 HDL2。 LDL和VLDL。此外。研究了不同因素对低密度脂蛋白粒子聚集和融合的影响。 LDL粒径不受添加高达300 mM NaCl和载体溶液pH从3.2增加到7.4的影响。但是用α-胰凝乳蛋白酶,鞘磷脂酶或硫酸铜处理LDL会导致聚集和融合的LDL颗粒形成。 (c)2006 Elsevier Inc.保留所有权利。

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