Zubarev Roman A, Witt Matthias, Baykut Gökhan
Laboratory for Biological and Medical Mass Spectrometry, Uppsala University, Sweden.
Anal Chem. 2005 May 1;77(9):2992-6. doi: 10.1021/ac048531j.
A new technique called selective excitation of ions for consecutive activation (SEICA) is proposed for obtaining complementary fragmentation mass spectra from the same precursor ion population. SEICA utilizes precursor ions remaining intact after electron capture dissociation or another ion-electron reaction for efficient MS/MS based on a vibrational excitation (VE) technique, such as infrared multiphoton dissociation. SEICA uses the ability of ion-trapping instruments to detect product ions while retaining inside the trap intact precursor ions, making the latter available for consecutive activation by a VE technique. The possibility of practical implementation of SEICA by software-only modification of a commercial instrument is demonstrated. A 2-fold increase in the efficiency is achieved for both "single-scan" and "multiple-scan" experiments. This improvement can be particularly important for high-sensitivity applications in, for example, proteomics, where limited ECD efficiency poses an obstacle for broad implementation of this technique.
提出了一种名为连续激活离子选择性激发(SEICA)的新技术,用于从同一前体离子群体中获得互补的碎裂质谱。SEICA利用电子捕获解离或其他离子-电子反应后保持完整的前体离子,基于振动激发(VE)技术(如红外多光子解离)进行高效的串联质谱分析。SEICA利用离子阱仪器在阱内保留完整前体离子的同时检测产物离子的能力,使后者可通过VE技术进行连续激活。通过对商用仪器仅进行软件修改来实际实现SEICA的可能性得到了证明。在“单扫描”和“多扫描”实验中,效率都提高了两倍。这种改进对于例如蛋白质组学中的高灵敏度应用可能特别重要,在蛋白质组学中,有限的电子捕获解离效率对该技术的广泛应用构成了障碍。