Ion trap mass spectrometry as detector for capillary electrochromatography of peptides: Possibilities and limitations

Marco Gaspari, Marjan Guček, Karin Walhagen, Rob J. Vreeken, Elwin R. Verheij, Ubbo R. Tjaden, Jan Van der Greef
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引用次数: 13

Abstract

Capillary electrochromatography has been coupled to an ion trap mass spectrometer via a sheath flow electrospray interface. Peptide analysis was performed on 25 cm columns packed with C18-bonded silica particles, and very fast separations were obtained. Full mass spectrometry and tandem mass spectrometry (MS/MS) detection were evaluated in terms of sensitivity and scanning speed. The separation of seven selected peptides and their detection by MS/MS in selected reaction monitoring mode was demonstrated. The performance of this sheath flow interface also was compared with the previously reported sheathless interface. Despite the loss in sensitivity (20–40-fold), the sheath flow interface was shown to be superior in terms of ruggedness, and allowed the use of higher electric fields to achieve faster analysis times. © 2001 John Wiley & Sons, Inc. J Micro Sep 13: 243–249, 2001

离子阱质谱法作为多肽毛细管电色谱的检测器:可能性和局限性
毛细管电色谱已耦合到离子阱质谱仪通过鞘流电喷雾界面。在填充c18键合二氧化硅颗粒的25 cm柱上进行多肽分析,获得了非常快速的分离。对全质谱法和串联质谱法(MS/MS)检测的灵敏度和扫描速度进行评价。在选择的反应监测模式下,演示了7种选定肽的分离和MS/MS检测。该护套流动界面的性能也与之前报道的无护套流动界面进行了比较。尽管灵敏度下降(20 - 40倍),但护套流动界面在坚固性方面表现出色,并允许使用更高的电场来实现更快的分析时间。©2001 John Wiley &[J] .中国科技大学学报(自然科学版),2001
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