Critical assessment of alignment procedures for LC- MS proteomics and metabolomics measurements

被引:131
作者
Lange, Eva [1 ]
Tautenhahn, Ralf [2 ]
Neumann, Steffen [2 ]
Groepl, Clemens [3 ]
机构
[1] Beatson Inst Canc Res, Prote & Mass Spectrometry Grp, Glasgow G61 1BD, Lanark, Scotland
[2] Leibniz Inst Plant Biochem Bioinformat & Mass Spe, Halle, Germany
[3] Free Univ Berlin, Dept Math & Comp Sci, D-1000 Berlin, Germany
关键词
D O I
10.1186/1471-2105-9-375
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Liquid chromatography coupled to mass spectrometry (LC-MS) has become a prominent tool for the analysis of complex proteomics and metabolomics samples. In many applications multiple LC-MS measurements need to be compared, e. g. to improve reliability or to combine results from different samples in a statistical comparative analysis. As in all physical experiments, LC-MS data are affected by uncertainties, and variability of retention time is encountered in all data sets. It is therefore necessary to estimate and correct the underlying distortions of the retention time axis to search for corresponding compounds in different samples. To this end, a variety of so-called LC-MS map alignment algorithms have been developed during the last four years. Most of these approaches are well documented, but they are usually evaluated on very specific samples only. So far, no publication has been assessing different alignment algorithms using a standard LC-MS sample along with commonly used quality criteria. Results: We propose two LC-MS proteomics as well as two LC-MS metabolomics data sets that represent typical alignment scenarios. Furthermore, we introduce a new quality measure for the evaluation of LC-MS alignment algorithms. Using the four data sets to compare six freely available alignment algorithms proposed for the alignment of metabolomics and proteomics LC-MS measurements, we found significant differences with respect to alignment quality, running time, and usability in general. Conclusion: The multitude of available alignment methods necessitates the generation of standard data sets and quality measures that allow users as well as developers to benchmark and compare their map alignment tools on a fair basis. Our study represents a first step in this direction. Currently, the installation and evaluation of the "correct" parameter settings can be quite a time-consuming task, and the success of a particular method is still highly dependent on the experience of the user. Therefore, we propose to continue and extend this type of study to a community-wide competition. All data as well as our evaluation scripts are available at http://msbi.ipb-halle.de/msbi/caap.
引用
收藏
页数:19
相关论文
共 40 条
[1]   Comparative LC-MS: A landscape of peaks and valleys [J].
America, Antoine H. P. ;
Cordewener, Jan H. G. .
PROTEOMICS, 2008, 8 (04) :731-749
[2]  
*ARGF IPRG, 2008, ABRF2008 S SALT LAK
[3]   A suite of algorithms for the comprehensive analysis of complex protein mixtures using high-resolution LC-MS [J].
Bellew, Matthew ;
Coram, Marc ;
Fitzgibbon, Matthew ;
Igra, Mark ;
Randolph, Tim ;
Wang, Pei ;
May, Damon ;
Eng, Jimmy ;
Fang, Ruihua ;
Lin, ChenWei ;
Chen, Jinzhi ;
Goodlett, David ;
Whiteaker, Jeffrey ;
Paulovich, Amanda ;
McIntosh, Martin .
BIOINFORMATICS, 2006, 22 (15) :1902-1909
[4]   Quantitative profiling of the membrane proteome in a halophilic archaeon [J].
Bisle, Birgit ;
Schmidt, Alexander ;
Scheibe, Burghardt ;
Klein, Christian ;
Tebbe, Andreas ;
Kellermann, Joseph ;
Siedler, Frank ;
Pfeiffer, Friedhelm ;
Lottspeich, Friedrich ;
Oesterhelt, Dieter .
MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (09) :1543-1558
[5]   Metabolome analysis of Biosynthetic mutants reveals a diversity of metabolic changes and allows identification of a large number of new compounds in arabidopsis [J].
Boettcher, Christoph ;
von Roepenack-Lahaye, Edda ;
Schmidt, Juergen ;
Schmotz, Constanze ;
Neumann, Steffen ;
Scheel, Dierk ;
Clemens, Stephan .
PLANT PHYSIOLOGY, 2008, 147 (04) :2107-2120
[6]   PARAFAC. Tutorial and applications [J].
Bro, R .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 1997, 38 (02) :149-171
[7]   Chromatographic alignment by warping and dynamic programming as a pre-processing tool for PARAFAC modelling of liquid chromatography-mass spectrometry data [J].
Bylund, D ;
Danielsson, R ;
Malmquist, G ;
Markides, KE .
JOURNAL OF CHROMATOGRAPHY A, 2002, 961 (02) :237-244
[8]   Hierarchical metabolomics demonstrates substantial compositional similarity between genetically modified and conventional potato crops [J].
Catchpole, GS ;
Beckmann, M ;
Enot, DP ;
Mondhe, M ;
Zywicki, B ;
Taylor, J ;
Hardy, N ;
Smith, A ;
King, RD ;
Kell, DB ;
Fiehn, O ;
Draper, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (40) :14458-14462
[9]   Introduction to computational proteomics [J].
Colinge, Jacques ;
Bennett, Keiryn L. .
PLOS COMPUTATIONAL BIOLOGY, 2007, 3 (07) :1151-1160
[10]   Current trends and future requirements for the mass spectrometric investigation of microbial, mammalian and plant metabolomes [J].
Dunn, Warwick B. .
PHYSICAL BIOLOGY, 2008, 5 (01)