Horigome T, Hiranuma T, Sugano H
Department of Biochemistry, Faculty of Science, Niigata University, Japan.
Eur J Biochem. 1989 Dec 8;186(1-2):63-9. doi: 10.1111/j.1432-1033.1989.tb15178.x.
Ceramic hydroxyapatite high-performance liquid chromatography was examined as a chromatographic method by which complexes of whole membrane proteins and sodium dodecyl sulfate could be analyzed. The chromatographic conditions were optimized using the erythrocyte membrane as a model. Whole proteins, including membrane proteins larger than 100 kDa, were eluted as sharp peaks from the column and separated well from each other under optimum conditions. This method gave better resolution of protein-SDS complexes than other chromatographic methods reported so far. The sodium dodecyl sulfate complexes of 24 well characterized proteins were analyzed by this method and their retention times were examined. The positive correlation of the retention time with log (molecular mass) and log sigma (hydrophobicity of amino acids) but not with the isoelectric point, was observed. Based on these results, the mechanism underlying the interaction of protein-SDS complexes with ceramic hydroxyapatite was discussed.
研究了陶瓷羟基磷灰石高效液相色谱法,以此作为一种可分析全膜蛋白与十二烷基硫酸钠复合物的色谱方法。以红细胞膜为模型对色谱条件进行了优化。包括大于100 kDa的膜蛋白在内的全蛋白在最佳条件下从柱中以尖锐峰形洗脱,且彼此分离良好。该方法对蛋白 - SDS复合物的分离效果优于目前报道的其他色谱方法。用此方法分析了24种特征明确的蛋白质的十二烷基硫酸钠复合物,并检测了它们的保留时间。观察到保留时间与log(分子量)和log σ(氨基酸疏水性)呈正相关,但与等电点无关。基于这些结果,讨论了蛋白 - SDS复合物与陶瓷羟基磷灰石相互作用的潜在机制。