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Rapid and efficient proteolysis through laser-assisted immobilized enzyme reactors

机译:通过激光辅助固定化酶反应器快速有效地进行蛋白水解

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摘要

In this report, laser radiation (808. nm) for the first time was employed to enhance the efficiency of proteolysis through immobilized enzyme reactor (IMER). IMER based monolithic support was prepared in the fused-silica capillary via a simple two-step procedure including acryloylation on trypsin surface and in situ aqueous polymerization/immobilization. The feasibility and high efficiency of the laser-assisted IMER were demonstrated by the digestion of bovine serum albumin (BSA), cytochrome c (Cyt-c) and β-casein. The digestion process was achieved in 60. s. The peptides were identified by MALDI-TOF-MS, yielding the sequence coverage of 33% for BSA, 73% for Cyt-c and 22% for β-casein. The comparisons between the in-solution digestion and on IMER reaction with/without laser assistance were made. To further confirm its efficiency in proteome analysis, the laser-assisted IMER was also applied to the analysis of one fraction of human serum sample through two-dimensional (2-D) separation of strong anion exchange/reversed-phase liquid chromatography (SAX/RPLC). After a database search, 49 unique peptides corresponding to 5 proteins were identified. The results showed that the laser-assisted IMER provides a promising platform for the high-throughput protein identification.
机译:在此报告中,首次采用激光辐射(808. nm)来提高通过固定化酶反应器(IMER)进行蛋白水解的效率。通过简单的两步程序(包括胰蛋白酶表面上的丙烯酰化和原位水聚合/固定),在熔融石英毛细管中制备了基于IMER的整体式载体。牛血清白蛋白(BSA),细胞色素c(Cyt-c)和β-酪蛋白的消化证明了激光辅助IMER的可行性和高效率。消化过程在60秒内完成。通过MALDI-TOF-MS鉴定了这些肽,对BSA的序列覆盖率为33%,对Cyt-c的覆盖率为73%,对β-酪蛋白的覆盖率为22%。进行了溶液内消化和有/无激光辅助的IMER反应的比较。为了进一步确认其在蛋白质组分析中的效率,激光辅助IMER还通过强阴离子交换/反相液相色谱(SAX / RPLC)。在数据库搜索后,鉴定出对应于5种蛋白质的49个独特肽段。结果表明,激光辅助的IMER为高通量蛋白质鉴定提供了有希望的平台。

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