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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Functionalized magnetic carbonaceous microspheres for trypsin immobilization and the application to fast proteolysis
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Functionalized magnetic carbonaceous microspheres for trypsin immobilization and the application to fast proteolysis

机译:功能化磁性碳微球固定化胰蛋白酶及其在快速蛋白水解中的应用

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摘要

In this study, magnetic carbonaceous (MC) microspheres prepared with a large-scale synthesis approach were developed as the novel substrate for enzyme immobilization, and the trypsin-immobilized MC microspheres were successfully applied to protein fast digestion. Firstly, MC microspheres with small size, strong magnetism, and biological compatibility were prepared through two-step solvothermal reactions. Secondly, MC microsphere surface was modified by 3-glycidoxypropyltrimethoxysilane (GLYMO). Finally, the enzyme was immobilized on the GLYMO-functionalized MC microspheres. The enzyme-immobilized magnetic microspheres were applied for fast protein digestion with microwave-assistance. Bovine serum albumin, myoglobin and cytochrome c, were used as model proteins to verify the digestion efficiency, and the digestion products were then characterized using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) with sequence coverage of 43%, 90% and 77%, respectively. The enzyme-immobilized magnetic particles were also, successfully applied to the analysis of human pituitary extract. After database search, 485 proteins (p < 0.01) were identified when the extract was digested by the microspheres. This opens a route for its future application in bottom-up proteomic analysis.
机译:在这项研究中,开发了通过大规模合成方法制备的磁性碳质(MC)微球作为固定化酶的新型底物,并且胰蛋白酶固定的MC微球成功地用于蛋白质快速消化。首先,通过两步溶剂热反应制备了具有小尺寸,强磁性和生物相容性的MC微球。其次,MC微球表面被3-环氧丙氧基丙基三甲氧基硅烷(GLYMO)改性。最后,将酶固定在GLYMO功能化的MC微球上。固定有酶的磁性微球用于微波辅助快速蛋白质消化。牛血清白蛋白,肌红蛋白和细胞色素c被用作模型蛋白以验证消化效率,然后使用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)对消化产物进行表征。序列覆盖率分别为43%,90%和77%。固定有酶的磁性颗粒也成功地用于人垂体提取物的分析。在数据库搜索后,当提取物被微球消化时,鉴定出485种蛋白质(p <0.01)。这为将来在自下而上的蛋白质组学分析中的应用开辟了道路。

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