An insight into iTRAQ: where do we stand now?

The iTRAQ (isobaric tags for relative and absolute quantification) technique is widely employed in proteomic workflows requiring relative quantification. Here, we review the iTRAQ literature; in particular, we focus on iTRAQ usage in relation to other commonly used quantitative techniques e.g. stabl...

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Veröffentlicht in:Analytical and bioanalytical chemistry 2012-09, Vol.404 (4), p.1011-1027
Hauptverfasser: Evans, Caroline, Noirel, Josselin, Ow, Saw Yen, Salim, Malinda, Pereira-Medrano, Ana G., Couto, Narciso, Pandhal, Jagroop, Smith, Duncan, Pham, Trong Khoa, Karunakaran, Esther, Zou, Xin, Biggs, Catherine A., Wright, Phillip C.
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Sprache:eng
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Zusammenfassung:The iTRAQ (isobaric tags for relative and absolute quantification) technique is widely employed in proteomic workflows requiring relative quantification. Here, we review the iTRAQ literature; in particular, we focus on iTRAQ usage in relation to other commonly used quantitative techniques e.g. stable isotope labelling in culture (SILAC), label-free methods and selected reaction monitoring (SRM). As a result, we identify several issues arising with respect to iTRAQ. Perhaps frustratingly, iTRAQ’s attractiveness has been undermined by a number of technical and analytical limitations: it may not be truly quantitative, as the changes in abundance reported will generally be underestimated. We discuss weaknesses and strengths of iTRAQ as a methodology for relative quantification in the light of this and other technical issues. We focus on technical developments targeted at iTRAQ accuracy and precision, use of 4-plex over 8-plex reagents and application of iTRAQ to post-translational modification (PTM) workflows. We also discuss iTRAQ in relation to label-free approaches, to which iTRAQ is losing ground. Figure  
ISSN:1618-2642
1618-2650
DOI:10.1007/s00216-012-5918-6