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首页> 外文期刊>Analytical and bioanalytical chemistry >Penetrable silica microspheres for immobilization of bovine serum albumin and their application to the study of the interaction between imatinib mesylate and protein by frontal affinity chromatography
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Penetrable silica microspheres for immobilization of bovine serum albumin and their application to the study of the interaction between imatinib mesylate and protein by frontal affinity chromatography

机译:渗透性硅胶微球固定牛血清白蛋白及其在额叶亲和色谱研究甲磺酸伊马替尼与蛋白质相互作用中的应用

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In the current study, novel featured silica, named penetrable silica, simultaneously containing macropores and mesopores, was immobilized with bovine serum albumin (BSA) via Schiff base method. The obtained BSA-SiO2 was employed as the high-performance liquid chromatographic (HPLC) stationary phase. Firstly, d- and l-tryptophan were used as probes to investigate the chiral separation ability of the BSA-SiO2 stationary phase. An excellent enantioseparation factor was obtained up to 4.3 with acceptable stability within at least 1 month. Next, the BSA-SiO2 stationary phase was applied to study the interaction between imatinib mesylate (IM) and BSA by frontal affinity chromatography. A single type of binding site was found for IM with the immobilized BSA, and the hydrogen-bonding and van der Waals interactions were expected to be contributing interactions based on the thermodynamic studies, and this was a spontaneous process. Compared to the traditional silica for HPLC stationary phase, the proposed penetrable silica microsphere possessed a larger capacity to bond more BSA, minimizing column overloading effects and enhancing enantioseparation ability. In addition, the lower running column back pressure and fast mass transfer were meaningful for the column stability and lifetime. It was a good substrate to immobilize biomolecules for fast chiral resolution and screening drug-protein interactions.
机译:在当前的研究中,通过席夫碱法将牛血清白蛋白(BSA)固定了同时具有大孔和中孔的新型特征二氧化硅,称为可渗透二氧化硅。所获得的BSA-SiO 2被用作高效液相色谱(HPLC)固定相。首先,以d-色氨酸和l-色氨酸为探针,研究了BSA-SiO2固定相的手性分离能力。至少在1个月内获得了优良的对映体分离因子,其稳定性高达4.3。接下来,采用BSA-SiO2固定相通过额叶亲和色谱研究甲磺酸伊马替尼(IM)与BSA之间的相互作用。基于固定化的BSA,发现IM具有单一类型的结合位点,并且基于热力学研究,氢键和范德华相互作用预计将促进相互作用,这是一个自发过程。与用于HPLC固定相的传统硅胶相比,该可穿透的硅胶微球具有更大的键合更多BSA的能力,从而最大程度地减少了色谱柱超载作用并增强了对映分离能力。此外,较低的运行柱背压和快速传质对于色谱柱的稳定性和使用寿命至关重要。它是固定生物分子以实现快速手性拆分和筛选药物-蛋白质相互作用的良好底物。

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