Department of Pharmaceutical Chemistry, Mass Spectrometry Facility, University of California, San Francisco, California 94158, USA.
Anal Chem. 2010 Jan 15;82(2):579-84. doi: 10.1021/ac9018582.
It is well established that protein sequence determination may be achieved by mass spectrometric analysis of protonated tryptic peptides subjected to collisional activation. When separated by nanoflow HPLC, a high percentage of peptides from complex mixtures of proteins can usually be identified. Recently, alternative, radical-driven fragmentation approaches of electron capture dissociation and the more common electron transfer dissociation (ETD) have been introduced and made widely available. In order to utilize these techniques in large scale proteomics studies, it is important to characterize the performance of these fragmentation processes on peptides formed by a range of enzymatic cleavages. In this study, we present a statistical analysis of the ion types that are observed from peptides produced by different enzymes and highlight the different characteristics of ETD spectra of doubly charged precursors in comparison to precursors of higher charge states.
已经证实,通过对经质子化的胰蛋白酶肽进行碰撞激活的质谱分析,可以实现蛋白质序列测定。当通过纳流高效液相色谱法分离时,通常可以鉴定出来自复杂蛋白质混合物的高比例肽。最近,已经引入了替代的、自由基驱动的电子捕获解离和更常见的电子转移解离(ETD)的碎片化方法,并广泛应用。为了在大规模蛋白质组学研究中利用这些技术,重要的是要对由一系列酶切形成的肽的这些碎片化过程的性能进行特征描述。在这项研究中,我们对不同酶产生的肽所观察到的离子类型进行了统计分析,并强调了与更高电荷状态的前体相比,双电荷前体的 ETD 光谱的不同特征。