Shao Chen, Gao Youhe
Department of Physiology and Pathophysiology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
Se Pu. 2010 Feb;28(2):128-34. doi: 10.3724/sp.j.1123.2012.00128.
Liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) has been one of the most popular approaches in proteome analysis. As an independent parameter to mass spectrometry information, peptide retention time has been utilized to facilitate protein identification and quantification. In the field of peptide identification, the prediction of the retention time combined with routine tandem mass spectrometry database searching methods could help improve the confidence of identification. The sensitivity of identification could also be improved by matching peaks with both the accurate mass and retention time in multiple aligned LC-MS runs. Meanwhile, because small changes of liquid chromatography conditions lead to variability in retention times unavoidably, retention time alignment is crucial to label-free quantification. Additionally, post-translational modifications (PTM) could be identified by combining retention time shifts and mass deviation information.
液相色谱-串联质谱联用(LC-MS/MS)一直是蛋白质组分析中最常用的方法之一。作为质谱信息的一个独立参数,肽段保留时间已被用于促进蛋白质的鉴定和定量。在肽段鉴定领域,结合常规串联质谱数据库搜索方法预测保留时间有助于提高鉴定的可信度。通过在多次对齐的LC-MS运行中将峰与精确质量和保留时间进行匹配,也可以提高鉴定的灵敏度。同时,由于液相色谱条件的微小变化不可避免地会导致保留时间的变化,保留时间对齐对于无标记定量至关重要。此外,通过结合保留时间偏移和质量偏差信息可以鉴定翻译后修饰(PTM)。