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Stabilized enzyme immobilization on micron-size PSt–GMA microspheres: different methods to improve the carriers' surface biocompatibility

机译:微米尺寸PST-GMA微球上稳定的酶固定化:改善载体表面生物相容性的不同方法

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Stabilized immobilization of biomacromolecules on carriers with appropriate orientation and minimum conformational changes is very important in the biochemical and biomedical fields. In this study, PSt–GMA(polystyrene–glycidyl methacrylate) microspheres were utilized as the carriers of immobilizing glucose oxidase (GOD). To improve the carrier's biocompatibility, anionic sulfonate groups and different length of spacer arms were introduced onto the microspheres' surface. The effect of carrier surface properties on the activity and stability of immobilized enzymes was investigated. The results show that the introduction of sulfonate groups and spacer arms could effectively reduce the unspecific adsorption of enzymes and improve their stabilities. Besides, with the increase of the length of spacer arms, both the immobilization amount and stabilities of immobilized GOD could be increased under different experimental conditions.
机译:在具有适当取向和最小构象变化的载体上稳定的生物致摩托的固体化在生物化学和生物医学领域非常重要。在该研究中,PST-GMA(聚苯乙烯 - 甲基丙烯酸酯)微球作为固定葡萄糖氧化酶(上帝)的载体。为了改善载体的生物相容性,将阴离子磺酸盐基团和不同长度的间隔臂引入微球表面上。研究了载体表面性质对固定化酶活性和稳定性的影响。结果表明,磺酸盐基团和间隔臂的引入可以有效地降低酶的非特异性吸附并改善它们的稳定性。此外,随着间隔臂的长度的增加,在不同的实验条件下可以增加固定的上帝的固定量和稳定性。

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