Analytical and Bioanalytical Chemistry

, Volume 405, Issue 17, pp 5663–5670

Detection and quantification of proteins and cells by use of elemental mass spectrometry: progress and challenges


DOI: 10.1007/s00216-013-6886-1

Cite this article as:
Yan, X., Yang, L. & Wang, Q. Anal Bioanal Chem (2013) 405: 5663. doi:10.1007/s00216-013-6886-1


Much progress has been made in identification of the proteins in proteomes, and quantification of these proteins has attracted much interest. In addition to popular tandem mass spectrometric methods based on soft ionization, inductively coupled plasma mass spectrometry (ICPMS), a typical example of mass spectrometry based on hard ionization, usually used for analysis of elements, has unique advantages in absolute quantification of proteins by determination of an element with a definite stoichiometry in a protein or attached to the protein. In this Trends article, we briefly describe state-of-the-art ICPMS-based methods for quantification of proteins, emphasizing protein-labeling and element-tagging strategies developed on the basis of chemically selective reactions and/or biospecific interactions. Recent progress from protein to cell quantification by use of ICPMS is also discussed, and the possibilities and challenges of ICPMS-based protein quantification for universal, selective, or targeted quantification of proteins and cells in a biological sample are also discussed critically. We believe ICPMS-based protein quantification will become ever more important in targeted quantitative proteomics and bioanalysis in the near future.

Online Abstract Figure

ICPMS-based protein and cell quantification


ICPMS Protein quantification Cell quantification 

Copyright information

© Springer-Verlag Berlin Heidelberg 2013

Authors and Affiliations

  1. 1.Department of Chemistry and the Key Laboratory of Analytical Science, College of Chemistry and Chemical EngineeringXiamen UniversityXiamenChina
  2. 2.State Key Laboratory of Marine Environmental ScienceXiamen UniversityXiamenChina

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