Park Sung-Gun, Mohr Jared P, Anderson Gordon A, Bruce James E
Department of Genome Sciences, University of Washington, Seattle, WA 98109.
GAA Custom Engineering, LLC, Benton City, WA 99320.
Int J Mass Spectrom. 2021 Jul;465. doi: 10.1016/j.ijms.2021.116578. Epub 2021 Mar 19.
Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) coupled with liquid chromatography (LC) is a powerful combination useful in many research areas due to the utility of high mass resolving power and mass measurement accuracy for studying highly complex samples. Ideally, every analyte in a complex sample can be subjected to accurate mass MS/MS analysis to aid in identification. FT-ICR MS can provide high mass resolving power and mass accuracy at the cost of long data acquisition periods, reducing the number of spectra that can be acquired per unit time. Frequency multiple signal acquisition has long been realized as an attractive method to obtain high mass resolving power and mass accuracy with shorter data acquisition periods. However, one of the limitations associated with frequency multiple signal acquisition is reduced signal intensity as compared to a traditional dipole detector. In this study, we demonstrated the use of a novel ICR cell to improve frequency multiple signal intensity and investigated the potential use of frequency multiple acquisition for proteome measurements. This novel ICR cell containing both dipole and frequency multiple detection electrodes was installed on a 7T FT-ICR MS coupled to an LC system. Tryptic digests of HeLa cell lysates were analyzed using dipole and frequency multiple detectors by holding either the mass resolving power or signal acquisition time constant. Compared to dipole detection, second frequency multiple detection yielded 36% or 45% more unique identified peptides from HeLa cell lysates at twice the scan rate or twice the mass resolving power, respectively. These results indicate that frequency multiple signal acquisition with either the same resolving power or the same signal acquisition duration as used with dipole signals can produce a significant increase in the number of peptides identified in complex proteome samples.
傅里叶变换离子回旋共振质谱(FT-ICR MS)与液相色谱(LC)联用,由于其在研究高度复杂样品时具有高质量分辨能力和质量测量准确性,在许多研究领域都是一种强大的组合。理想情况下,复杂样品中的每种分析物都可以进行精确质量的串联质谱(MS/MS)分析以辅助鉴定。FT-ICR MS能够提供高质量分辨能力和质量准确性,但代价是数据采集时间长,这减少了单位时间内可采集的光谱数量。频率多路信号采集长期以来一直被认为是一种有吸引力的方法,可在更短的数据采集时间内获得高质量分辨能力和质量准确性。然而,与频率多路信号采集相关的一个限制是与传统偶极检测器相比信号强度降低。在本研究中,我们展示了使用新型离子回旋共振(ICR)池来提高频率多路信号强度,并研究了频率多路采集在蛋白质组测量中的潜在用途。这种同时包含偶极和频率多路检测电极的新型ICR池安装在与液相色谱系统联用的7T FT-ICR MS上。通过保持质量分辨能力或信号采集时间恒定,使用偶极和频率多路检测器对HeLa细胞裂解物的胰蛋白酶消化产物进行分析。与偶极检测相比,第二次频率多路检测在扫描速率加倍或质量分辨能力加倍时,分别从HeLa细胞裂解物中鉴定出的独特肽段数量多36%或45%。这些结果表明,与偶极信号使用相同分辨能力或相同信号采集持续时间的频率多路信号采集,可以显著增加复杂蛋白质组样品中鉴定出的肽段数量。