共 40 条
Peptide Labeling with Isobaric Tags Yields Higher Identification Rates Using iTRAQ 4-Plex Compared to TMT 6-Plex and iTRAQ 8-Plex on LTQ Orbitrap
被引:149
作者:

Pichler, Peter
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机构:
Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria

Koecher, Thomas
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h-index: 0
机构:
Res Inst Mol Pathol, A-1030 Vienna, Austria Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria

Holzmann, Johann
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机构:
Res Inst Mol Pathol, A-1030 Vienna, Austria Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria

Mazanek, Michael
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h-index: 0
机构:
Res Inst Mol Pathol, A-1030 Vienna, Austria Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria

Taus, Thomas
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机构:
Res Inst Mol Pathol, A-1030 Vienna, Austria Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria

Ammerer, Gustav
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机构:
Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria
Univ Vienna, Max F Perutz Labs, A-1030 Vienna, Austria Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria

Mechtler, Karl
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h-index: 0
机构:
Inst Mol Biotechnol, Vienna, Austria Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria
机构:
[1] Univ Vienna, Christian Doppler Lab Proteome Anal, A-1030 Vienna, Austria
[2] Res Inst Mol Pathol, A-1030 Vienna, Austria
[3] Univ Vienna, Max F Perutz Labs, A-1030 Vienna, Austria
[4] Inst Mol Biotechnol, Vienna, Austria
关键词:
SPECTROMETRY-BASED PROTEOMICS;
TANDEM MASS-SPECTROMETRY;
COMPLEX PROTEIN MIXTURES;
QUANTITATIVE-ANALYSIS;
QUANTIFICATION;
PHOSPHORYLATION;
TRAP;
VALIDATION;
DISCOVERY;
STRATEGY;
D O I:
10.1021/ac100890k
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Peptide labeling with isobaric tags has become a popular technique in quantitative shotgun proteomics. Using two different samples viz, a protein mixture and He La extracts, we show that three commercially available isobaric tags differ with regard to peptide identification rates: The number of identified proteins and peptides was largest with iTRAQ 4-plex, followed by TMT 6-plex, and smallest with iTRAQ 8-plex. In all experiments, we employed a previously described method where two scans were acquired for each precursor on an LTQ Orbitrap: A CID scan under standard settings for identification, and a HCD scan for quantification. The observed differences in identification rates were similar when data was searched with either Mascot or Sequest. We consider these findings to be the result of a combination of several factors, most notably prominent ions in CID spectra as a consequence of loss of fragments of the label tag from precursor ions. These fragment ions cannot be explained by current search engines and were observed to have a negative impact on peptide scores.
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收藏
页码:6549 / 6558
页数:10
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