4.7 Review

An insight into iTRAQ: where do we stand now?

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 404, Issue 4, Pages 1011-1027

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-012-5918-6

Keywords

Shotgun proteomics; iTRAQ; Ratio underestimation; Relative quantification; MS/MS instrumentation; Isotopic impurities; Statistical validation; Modelling; PTMs; Label-free

Funding

  1. EPSRC [EP/E053556/1]
  2. ChELSI initiative [EP/E036252/1]
  3. EPSRC [EP/E036252/1, EP/E053556/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/E053556/1, EP/E036252/1] Funding Source: researchfish

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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.

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