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Development of Affinity Microcolumns for Drug-Protein Binding Studies in Personalized Medicine: Interactions of Sulfonylurea Drugs with in vivo Glycated Human Serum Albumin

机译:个性化医学中药物-蛋白质结合研究的亲和性微柱的开发:磺酰脲类药物与体内糖化人血清白蛋白的相互作用

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This report used high-performance affinity micro-columns to examine the changes in binding by sulfonylurea drugs to in vivo glycated HSA that had been isolated from individual patients with diabetes. An immunoextraction approach was developed to isolate HSA and glycated HSA from clinical samples, using only 20 μL of plasma or serum and 6-12 nmol of protein to prepare each affinity microcolumn. It was found that the affinity microcolumns could be used in either frontal analysis or zonal elution studies, which typically required only 4-8 min per run. The microcolumns had good stability and allowed data to be obtained for multiple drugs and experimental conditions over hundreds of sample application cycles. Both the overall binding, as measured by frontal analysis, and site-specific interactions, as examined by zonal elution, showed good agreement with previous data that had been obtained for in vitro glycated HSA with similar levels of modification. It was also possible to directly compare the changes in site-specific binding that occurred between sulfonylurea drugs or as the level of HSA glycation was varied. This method is not limited to clinical samples of glycated HSA but could be adapted for work with other modified proteins of interest in personalized medicine.
机译:该报告使用高性能亲和力微柱检查了磺酰脲类药物与体内糖化HSA的结合变化,而糖化HSA已从个别糖尿病患者中分离出来。开发了一种免疫提取方法,从临床样品中分离出HSA和糖化的HSA,仅使用20μL血浆或血清和6-12 nmol的蛋白质即可制备每个亲和力微柱。发现亲和微柱可用于额叶分析或区域洗脱研究,通常每次运行仅需4-8分钟。微柱具有良好的稳定性,可以在数百个样品应用周期内获得多种药物和实验条件的数据。通过额叶分析测量的整体结合,以及通过区域洗脱检测的位点特异性相互作用,都与以前的数据相似,这些数据与具有相似修饰水平的体外糖化HSA所获得的数据一致。也可以直接比较在磺酰脲类药物之间发生的位点特异性结合的变化,或随着HSA糖化水平的变化而发生的变化。该方法不仅限于糖化HSA的临床样品,还可以与个性化医学中其他感兴趣的修饰蛋白一起使用。

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