Comparison of data analysis parameters and MS/MS fragmentation techniques for quantitative proteome analysis using isobaric peptide termini labeling (IPTL)

被引:0
|
作者
Christian J. Koehler
Magnus Ø. Arntzen
Achim Treumann
Bernd Thiede
机构
[1] University of Oslo,The Biotechnology Centre of Oslo
[2] NEPAF,undefined
来源
关键词
CID; ETD; HCD; Isobaric labeling; IPTL; IsobariQ; MS/MS; Quantitative proteomics;
D O I
暂无
中图分类号
学科分类号
摘要
Isobaric peptide termini labeling (IPTL) is a quantification method which permits relative quantification using quantification points distributed throughout the whole tandem mass spectrometry (MS/MS) spectrum. It is based on the complementary derivatization of peptide termini with different isotopes resulting in isobaric peptides. Here, we use our recently developed software package IsobariQ to investigate how processing and data analysis parameters can improve IPTL data. Deisotoping provided cleaner MS/MS spectra and improved protein identification and quantification. Denoising should be used with caution because it may remove highly regulated ion pairs. An outlier detection algorithm on the ratios within every individual MS/MS spectrum was beneficial in removing false-positive quantification points. MS/MS spectra using IPTL typically contain two peptide series with complementary labels resulting in lower Mascot ion scores than non-labeled equivalent peptides. To avoid this penalty, the two chemical modifications for IPTL were specified as variables including satellite neutral losses of tetradeuterium with positive loss for the heavy isotopes and negative loss for the light isotopes. Thus, the less dominant complementary ion series were not considered for the scoring, which improved the ion scores significantly. In addition, we showed that IPTL was suitable for fragmentation by electron transfer dissociation (ETD) and higher energy collisionally activated dissociation (HCD) besides the already reported collision-induced dissociation (CID). Notably, ETD and HCD data can be identified and quantified using IsobariQ. ETD outperformed CID and HCD only for charge states ≥4+ but yielded in total fewer protein identifications and quantifications. In contrast, the high-resolution information of HCD fragmented peptides provided most identification and quantification results using the same scan speed.
引用
收藏
页码:1103 / 1114
页数:11
相关论文
共 50 条
  • [21] Profiling new taxanes using LC/MS and LC/MS/MS substructural analysis techniques
    Kerns, EH
    Volk, KJ
    Hill, SE
    Lee, MS
    RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1995, 9 (15) : 1539 - 1545
  • [22] Improving Quantitative Accuracy and Precision of Isobaric Labeling Strategies for Quantitative Proteomics Using Multistage (MS3) Mass Spectrometry
    Schreiber, Emanuel M.
    AMERICAN LABORATORY, 2013, 45 (01) : 10 - 13
  • [23] Effect of 2MEGA labeling on membrane proteome analysis using LC-ESI QTOF MS
    Ji, Chengjie
    Lo, Andy
    Marcus, Sandra
    Li, Liang
    JOURNAL OF PROTEOME RESEARCH, 2006, 5 (10) : 2567 - 2576
  • [24] Comparison of CID versus ETD-based MS/MS fragmentation for the analysis of doubly derivatized steroids
    Juang, Yu-Min
    She, Tzu-Fang
    Chen, Hui-Yi
    Lai, Chien-Chen
    JOURNAL OF MASS SPECTROMETRY, 2013, 48 (12): : 1349 - 1356
  • [25] Global Network Analysis of the Renal Cortical Proteome in Diabetic Mice Using 180 Isotopic Labeling and 2D LC-MS/MS
    Starkey, Jonathan W.
    Zhao, Yingxin
    Haidacher, Sigmund J.
    Lejeune, Wanda S.
    Luxon, Bruce A.
    Denner, Larry
    Tilton, Ronald G.
    DIABETES, 2009, 58 : A213 - A213
  • [26] Global Quantitative Proteomic Profiling through 18O-labeling in Combination with MS/MS Spectra Analysis
    White, Carl A.
    Oey, Nicodemus
    Emili, Andrew
    JOURNAL OF PROTEOME RESEARCH, 2009, 8 (07) : 3653 - 3665
  • [27] Amino Acid Analysis of Peptides Using Isobaric-Tagged Isotope Dilution LC-MS/MS
    Woolfitt, Adrian R.
    Solano, Maria I.
    Williams, Tracie L.
    Pirkle, James L.
    Barr, John R.
    ANALYTICAL CHEMISTRY, 2009, 81 (10) : 3979 - 3985
  • [28] Doping control analysis of selected peptide hormones using LC-MS(/MS)
    Thevis, Mario
    Thomas, Andreas
    Schaenzer, Wilhelm
    FORENSIC SCIENCE INTERNATIONAL, 2011, 213 (1-3) : 35 - 41
  • [29] Dynamic quantitative analysis of the nucleolar proteome using an Isobaric Mass Tagging (IMT) approach
    Xie, B.
    Kershnar, E.
    Parman, C.
    Wang, R.
    Maloney, J.
    Papacoda, E.
    Guerra, C.
    Smith, C.
    Taylor, P.
    Latimer, D. R.
    Kaplan, P. M.
    Mattessich, M. J.
    Lizardi, P. M.
    MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (10) : S105 - S105
  • [30] Quantitative proteomic analysis of rat retina with experimental autoimmune uveitis based on tandem mass tag (TMT) peptide labeling coupled with LC-MS/MS
    Liu, Bin
    Yin, Xuewei
    Wei, Huixia
    Wang, Zhe
    Tang, Hongying
    Qiu, Yan
    Hao, Yixian
    Zhang, Xiuyan
    Bi, Hongsheng
    Guo, Dadong
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2020, 1153