Tandem Mass Tags:  A Novel Quantification Strategy for Comparative Analysis of Complex Protein Mixtures by MS/MS

Andrew Thompson, Jürgen Schäfer, Karsten Kuhn, Stefan Kienle, Josef Schwarz, Günter Schmidt, Thomas Neumann, and Christian Hamon*
Proteome Sciences, Coveham House, Downside Bridge Road, Cobham, Surrey, KT11 3EP, U.K., and Xzillion GmbH, Industriepark Hchst, Building G865a, 65929 Frankfurt am Main, Germany
Anal. Chem., 2003, 75 (8), pp 1895–1904
DOI: 10.1021/ac0262560
Publication Date (Web): March 1, 2003
Copyright © 2003 American Chemical Society

 Proteome Sciences.

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 Xzillion GmbH.

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*

 Corresponding author. Fax:  0049 69 30544302. E-mail:  Christian.Hamon@ xzillion.com.

Abstract

A novel MS/MS-based analysis strategy using isotopomer labels, referred to as “tandem mass tags” (TMTs), for the accurate quantification of peptides and proteins is described. The new tags are designed to ensure that identical peptides labeled with different TMTs exactly comigrate in all separations. The tags require novel methods of quantification analysis using tandem mass spectrometry. The new tags and analysis methods allow peptides from different samples to be identified by their relative abundance with greater ease and accuracy than other methods. The new TMTs permit simultaneous determination of both the identity and relative abundances of peptide pairs using a collision induced dissociation (CID)-based analysis method. Relative abundance measurements made in the MS/MS mode using the new tags are accurate and sensitive. Compared to MS-mode measurements, a very high signal-to-noise ratio is achieved with MS/MS based detection. The new tags should be applicable to a wide variety of peptide isolation methods.

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History

  • Published In Issue April 15, 2003
  • Received for review October 23, 2002. Accepted January 30, 2003.

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