Kusalik Anthony J
IEEE Trans Nanobioscience. 2015 Jun;14(4):478-484. doi: 10.1109/TNB.2015.2419194. Epub 2015 Apr 29.
With tandem mass spectrometry (MS/MS), spectra can be generated by various fragmentation techniques including collision-induced dissociation (CID), higher-energy collisional dissociation (HCD), electron capture dissociation (ECD), electron transfer dissociation (ETD) and so on. At the same time, de novo sequencing using multiple spectra from the same peptide generated by different fragmentation techniques is becoming popular in proteomics studies. The focus of this study is the use of paired spectra from CID (or HCD) and ECD (or ETD) fragmentation because of the complementarity between them. We present a de novo peptide sequencing framework for multiple tandem mass spectra, and apply it to paired spectra sequencing problem. The performance of the framework on paired spectra is compared to another successful method named pNovo+. The results show that our proposed method outperforms pNovo+ in terms of full length peptide sequencing accuracy on three pairs of experimental datasets, with the accuracy increasing up to 13.6% compared to pNovo+.
利用串联质谱法(MS/MS),可以通过各种碎裂技术生成谱图,包括碰撞诱导解离(CID)、高能碰撞解离(HCD)、电子捕获解离(ECD)、电子转移解离(ETD)等。同时,在蛋白质组学研究中,使用由不同碎裂技术生成的来自同一肽段的多个谱图进行从头测序正变得越来越普遍。由于CID(或HCD)与ECD(或ETD)碎裂之间具有互补性,本研究的重点是使用来自CID(或HCD)和ECD(或ETD)碎裂的配对谱图。我们提出了一种用于多个串联质谱图的从头肽段测序框架,并将其应用于配对谱图测序问题。将该框架在配对谱图上的性能与另一种名为pNovo+的成功方法进行了比较。结果表明,在三对实验数据集上,我们提出的方法在全长肽段测序准确性方面优于pNovo+,与pNovo+相比,准确性提高了13.6%。