Catch and measure-mass spectrometry-based immunoassays in biomarker research

Biochim Biophys Acta. 2014 May;1844(5):927-32. doi: 10.1016/j.bbapap.2013.09.010. Epub 2013 Sep 21.

Abstract

Mass spectrometry-based (MS) methods are effective tools for discovering protein biomarker candidates that can differentiate between physiological and pathophysiological states. Promising candidates are validated in studies comprising large patient cohorts. Here, targeted protein analytics are used to increase sample throughput. Methods involving antibodies, such as sandwich immunoassays or Western blots, are commonly applied at this stage. Highly-specific and sensitive mass spectrometry-based immunoassays that have been established in recent years offer a suitable alternative to sandwich immunoassays for quantifying proteins. Mass Spectrometric ImmunoAssays (MSIA) and Stable Isotope Standards and Capture by Anti-Peptide Antibodies (SISCAPA/iMALDI) are two prominent types of MS-based immunoassays in which the capture is done either at the protein or the peptide level. We present an overview of these emerging types of immunoassays and discuss their suitability for the discovery and validation of protein biomarkers. This article is part of a Special Issue entitled: Biomarkers: A Proteomic Challenge.

Keywords: Immunoaffinity MS; Mass spectrometry immunoassay; SISCAPA; TXP.

Publication types

  • Review

MeSH terms

  • Biomarkers / analysis*
  • Chromatography, Affinity / methods*
  • Disease*
  • Humans
  • Immunoassay / methods*
  • Mass Spectrometry / methods*
  • Pathology, Molecular*
  • Peptide Fragments / analysis
  • Proteins / metabolism*

Substances

  • Biomarkers
  • Peptide Fragments
  • Proteins