首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Using high-concentration trypsin-immobilized magnetic nanoparticles for rapid in situ protein digestion at elevated temperature
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Using high-concentration trypsin-immobilized magnetic nanoparticles for rapid in situ protein digestion at elevated temperature

机译:使用高浓度胰蛋白酶固定的磁性纳米颗粒在高温下快速原位消化蛋白质

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摘要

We describe an innovative approach - using a high concentration of trypsin-modified magnetic nanoparticles (TMNPs) - for the rapid and efficient digestion of proteins at elevated temperature. The required digestion time could be reduced to less than 10 s. After digestion, the TMNPs were collected magnetically from the sample solution for reuse and the digested peptides were characterized using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. Protein digestion was optimized when using the TMNPs (5 mu g/mu L) at 57 degrees C; a significantly high peptide coverage was achieved for protein identification (e.g., 98% for lysozyme). Although a high concentration of TMNPs was used for digestion, the short digestion time led to much lower amounts of trypsin peptides being produced through self-digestion. As a result, interference in the mass spectrometric detection of the peptide ions was reduced significantly. Copyright (c) 2007 John Wiley & Sons, Ltd.
机译:我们描述了一种创新的方法-使用高浓度的胰蛋白酶修饰的磁性纳米颗粒(TMNP)-在高温下快速有效地消化蛋白质。所需的消解时间可以减少到少于10秒。消化后,以磁性方式从样品溶液中收集TMNP,以备再用,并使用基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱对消化的肽进行表征。当在57摄氏度下使用TMNP(5μg /μL)时,蛋白质消化得到了优化;对于蛋白质鉴定,肽的覆盖率非常高(例如,溶菌酶的覆盖率为98%)。尽管使用高浓度的TMNP进行消化,但是较短的消化时间导致通过自消化产生的胰蛋白酶肽的量低得多。结果,显着降低了对肽离子进行质谱检测的干扰。版权所有(c)2007 John Wiley&Sons,Ltd.

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