Department of Chemistry, Wichita State University, 1845 Fairmount, Wichita, KS, 67260-0051, USA.
J Am Soc Mass Spectrom. 2016 Dec;27(12):2064-2070. doi: 10.1007/s13361-016-1498-6. Epub 2016 Sep 19.
Precise localization of post-translational modifications (PTMs) on proteins and peptides is an outstanding challenge in proteomics. While electron transfer dissociation (ETD) has dramatically advanced PTM analyses, mixtures of localization variants that commonly coexist in cells often require prior separation. Although differential or field asymmetric waveform ion mobility spectrometry (FAIMS) achieves broad variant resolution, the need for standards to identify the features has limited the utility of approach. Here we demonstrate full a priori characterization of variant mixtures by high-resolution FAIMS coupled to ETD and the procedures to systematically extract the FAIMS spectra for all variants from such data. Graphical Abstract ᅟ.
在蛋白质组学中,精确定位蛋白质和肽的翻译后修饰(PTMs)是一个巨大的挑战。虽然电子转移解离(ETD)极大地促进了 PTM 分析,但细胞中通常共存的定位变体混合物通常需要预先分离。尽管差分或场非对称波形离子淌度谱(FAIMS)实现了广泛的变体分辨率,但识别特征的标准需求限制了该方法的实用性。在这里,我们通过高分辨率 FAIMS 与 ETD 相结合,展示了对变体混合物的全面先验表征,以及从这些数据中系统地提取所有变体的 FAIMS 谱的程序。