Comparative Study of Targeted and Label-free Mass Spectrometry Methods for Protein Quantification

被引:5
作者
Ijsselstijn, Linda [1 ]
Stoop, Marcel P. [1 ]
Stingl, Christoph [1 ]
Smitt, Peter A. E. Sillevis [1 ]
Luider, Theo M. [1 ]
Dekker, Lennard J. M. [1 ]
机构
[1] Erasmus MC, Dept Neurol, Rotterdam, Netherlands
关键词
protein quantification; targeted; qual/quant; multiple reaction monitoring; mass spectrometry; ABSOLUTE QUANTIFICATION; QUANTITATIVE PROTEOMICS; SINGLE; ASSAYS;
D O I
10.1021/pr301221f
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We compared data acquired on an LTQ-Orbitrap MS used in a typical shotgun proteomics setting (optimized for protein identification) with data from a quadrupole ion trap MS operated in the MRM mode. Six relative abundant proteins were quantified in identical sets of serum and CSF samples by the following methods: a qual/quant method with and without use of internal standards and a quantitative method (MRM with use of internal standards). Comparison of these methods with an antibody-based method in CSF samples showed good linearity for both methods (R-2 of 0.961 and 0.971 for the qual/quant method with use of internal standards and the quantitative method, respectively). Besides its better linearity, the quantitative method was also more reproducible with lower CVs for all samples. Next to these comparisons we also explored why a qual/quant approach had typically a lower reproducibility compared to MRM analyses. We observed that modified peptides, or peptides with a cysteine or a methionine, yielded a significant increase in CV. Furthermore, a positive correlation was found between the length of the peptide and the CV. We conclude that qual/quant is an alternative for the quantification of abundant proteins and that the use of internal standards in qual/quant could be advantageous. Furthermore, the ongoing development in MS techniques increases the possibilities of qual/quant in protein quantification.
引用
收藏
页码:2005 / 2011
页数:7
相关论文
共 23 条
  • [1] Multi-site assessment of the precision and reproducibility of multiple reaction monitoring-based measurements of proteins in plasma
    Addona, Terri A.
    Abbatiello, Susan E.
    Schilling, Birgit
    Skates, Steven J.
    Mani, D. R.
    Bunk, David M.
    Spiegelman, Clifford H.
    Zimmerman, Lisa J.
    Ham, Amy-Joan L.
    Keshishian, Hasmik
    Hall, Steven C.
    Allen, Simon
    Blackman, Ronald K.
    Borchers, Christoph H.
    Buck, Charles
    Cardasis, Helene L.
    Cusack, Michael P.
    Dodder, Nathan G.
    Gibson, Bradford W.
    Held, Jason M.
    Hiltke, Tara
    Jackson, Angela
    Johansen, Eric B.
    Kinsinger, Christopher R.
    Li, Jing
    Mesri, Mehdi
    Neubert, Thomas A.
    Niles, Richard K.
    Pulsipher, Trenton C.
    Ransohoff, David
    Rodriguez, Henry
    Rudnick, Paul A.
    Smith, Derek
    Tabb, David L.
    Tegeler, Tony J.
    Variyath, Asokan M.
    Vega-Montoto, Lorenzo J.
    Wahlander, Asa
    Waldemarson, Sofia
    Wang, Mu
    Whiteaker, Jeffrey R.
    Zhao, Lei
    Anderson, N. Leigh
    Fisher, Susan J.
    Liebler, Daniel C.
    Paulovich, Amanda G.
    Regnier, Fred E.
    Tempst, Paul
    Carr, Steven A.
    [J]. NATURE BIOTECHNOLOGY, 2009, 27 (07) : 633 - U85
  • [2] Quantitative mass spectrometric multiple reaction monitoring assays for major plasma proteins
    Anderson, L
    Hunter, CL
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (04) : 573 - 588
  • [3] SINGLE AND MULTIPLE ION RECORDING TECHNIQUES FOR ANALYSIS OF DIPHENYLHYDANTOIN AND ITS MAJOR METABOLITE IN PLASMA
    BATY, JD
    ROBINSON, PR
    [J]. BIOMEDICAL MASS SPECTROMETRY, 1977, 4 (01): : 36 - 41
  • [4] Specific peptides identified by mass spectrometry in placental tissue from pregnancies complicated by early onset preeclampsia attained by laser capture dissection
    de Groot, Christianne J. M.
    Guzel, Coskun
    Steegers-Theunissen, Regine P. M.
    de Maat, M.
    Derkx, Pieter
    Roes, Eva-Maria
    Heeren, Ron M. A.
    Luider, Theo M.
    Steegers, Eric A. P.
    [J]. PROTEOMICS CLINICAL APPLICATIONS, 2007, 1 (03) : 325 - 335
  • [5] Multiple reaction monitoring of mTRAQ-labeled peptides enables absolute quantification of endogenous levels of a potential cancer marker in cancerous and normal endometrial tissues
    DeSouza, Leroi V.
    Taylor, Adrian M.
    Li, Wei
    Minkoff, Marjorie S.
    Romaschin, Alexander D.
    Colgan, Terence J.
    Siu, K. W. Michael
    [J]. JOURNAL OF PROTEOME RESEARCH, 2008, 7 (08) : 3525 - 3534
  • [6] Options and considerations when selecting a quantitative proteomics strategy
    Domon, Bruno
    Aebersold, Ruedi
    [J]. NATURE BIOTECHNOLOGY, 2010, 28 (07) : 710 - 721
  • [7] Targeted Proteomic Quantification on Quadrupole-Orbitrap Mass Spectrometer
    Gallien, Sebastien
    Duriez, Elodie
    Crone, Catharina
    Kellmann, Markus
    Moehring, Thomas
    Domon, Bruno
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2012, 11 (12) : 1709 - 1723
  • [8] Selected reaction monitoring applied to proteomics
    Gallien, Sebastien
    Duriez, Elodie
    Domon, Bruno
    [J]. JOURNAL OF MASS SPECTROMETRY, 2011, 46 (03): : 298 - 312
  • [9] Proteomics on an Orbitrap Benchtop Mass Spectrometer Using All-ion Fragmentation
    Geiger, Tamar
    Cox, Juergen
    Mann, Matthias
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (10) : 2252 - 2261
  • [10] Absolute quantification of proteins and phosphoproteins from cell lysates by tandem MS
    Gerber, SA
    Rush, J
    Stemman, O
    Kirschner, MW
    Gygi, SP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (12) : 6940 - 6945