Absolute quantification of the model biomarker prostate-specific antigen in serum by LC-MS/MS using protein cleavage and isotope dilution mass spectrometry

David R. Barnidge, Marcia K. Goodmanson, George G. Klee, David C. Muddiman

Research output: Contribution to journalArticle

236 Citations (Scopus)

Abstract

Protein cleavage-isotope dilution mass spectrometry (PC-IDMS) can be used to quantify proteins, with an isotope-labeled analogue of the peptide fragment used as an internal standard. Here, we investigate use of a standard LC-MS/MS platform for quantifying a model biomarker directly from serum by this technique. We synthesized a peptide (IVGGWECEK) identical to the N-terminal tryptic fragment of PSA but with each glycine containing two 13C atoms and one 15N atom. PSA-free human serum was denatured with urea followed by the introduction of PSA standard and the stable isotope labeled internal standard peptide. The sample was then proteolyzed with trypsin and subjected to quantification using LC-MS/ MS on a triple quadrupole mass spectrometer. A linear least squares calibration curve made from five different concentrations of PSA added to serum and digested (each made in triplicate and randomly injected three times) had a mean slope of 0.973 (SE = 0.023), intercept of -0.003 (SE = 0.022), and R2 of 0.971. Recovery of calibrators ranged from 70 to 85% with a mean run-to-run CV of 13% and a mean within-run CV of 5.7%. PC-IDMS is a promising technique for quantifying proteins covering a broad range of applications from standardizing immunoassaysto monitoring post-translational modifications to quantifying newly discovered biomarkers prior to the development and implementation of an immunoassay, just to name a few. Issues surrounding the application of PC-IDMS for the absolute quantification of proteins include selection of a proteolytic fragment for quantification that can be cleaved and isolated reproducibly over a broad dynamic range, stable isotope labeled synthetic peptide standards that give consistent results, and LC-MS/MS methods that provide adequate sensitivity and reproducibility without creating impractical analysis times. The results presented here show that absolute quantification can be performed on the model biomarker PSA introduced into denatured serum when analyzed by LC-MS/MS. However, concerns still exist regarding sensitivity compared to existing immunoassays as well as the reproducibility of PC-IDMS performed in different matrixes.

Original languageEnglish (US)
Pages (from-to)644-652
Number of pages9
JournalJournal of Proteome Research
Volume3
Issue number3
DOIs
StatePublished - May 2004

Fingerprint

Biomarkers
Prostate-Specific Antigen
Isotopes
Dilution
Mass spectrometry
Mass Spectrometry
Serum
Proteins
Immunoassay
Peptides
Atoms
Peptide Fragments
Mass spectrometers
Post Translational Protein Processing
Least-Squares Analysis
Glycine
Trypsin
Calibration
Names
Urea

Keywords

  • Absolute quantification
  • Biomarker
  • LC-MS/MS
  • Prostate-specific antigen
  • Protein
  • Serum

ASJC Scopus subject areas

  • Genetics
  • Biotechnology
  • Biochemistry

Cite this

Absolute quantification of the model biomarker prostate-specific antigen in serum by LC-MS/MS using protein cleavage and isotope dilution mass spectrometry. / Barnidge, David R.; Goodmanson, Marcia K.; Klee, George G.; Muddiman, David C.

In: Journal of Proteome Research, Vol. 3, No. 3, 05.2004, p. 644-652.

Research output: Contribution to journalArticle

Barnidge, David R. ; Goodmanson, Marcia K. ; Klee, George G. ; Muddiman, David C. / Absolute quantification of the model biomarker prostate-specific antigen in serum by LC-MS/MS using protein cleavage and isotope dilution mass spectrometry. In: Journal of Proteome Research. 2004 ; Vol. 3, No. 3. pp. 644-652.
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