An antibody-free LC-MS/MS method for the quantification of sex hormone binding globulin in human serum and plasma

Bas Sleumer, Jordan Zwerwer, Martijn Van Faassen, Michel J. Vos, Rainer Bischoff, Ido P. Kema, Nico C. Van De Merbel*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

4 Citations (Scopus)
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Abstract

Sex hormone binding globulin (SHBG) is a hormone binding protein which plays an important role in regulating the transport and availability of biologically active androgens and estradiol to target cells and used to calculate free testosterone concentrations. A liquid chromatography-Tandem mass spectrometry (LC-MS/MS) method was developed, featuring an albumin removal step followed by a tryptic digestion. After a reduction step with dithiothreitol and alkylation with iodoacetamide three signature peptides were used for the quantification of SHBG. The method enables the quantification of serum and plasma SHBG over the clinically relevant range of 200-20,000 ng/mL and was validated according to the most recent guidelines. The LC-MS/MS method correlates well with the Abbott Alinity immunoassay (R2>0.95), but the LC-MS/MS results are on average 16-17% lower than the immunoassay results, which is consistent for all three signature peptides. The LC-MS/MS method which includes an albumin depletion step allows quantification of SHBG in serum and plasma without an immunocapture step at clinically relevant SHBG levels, thus contributing to better lab-To-lab consistency of results.

Original languageEnglish
Pages (from-to) 1266–1274
Number of pages9
JournalClinical chemistry and laboratory medicine
Volume61
Issue number7
Early online date13-Feb-2023
DOIs
Publication statusPublished - 2023

Keywords

  • albumin depletion
  • biomarker
  • human sex hormone binding globulin (SHBG)
  • liquid chromatography-Tandem mass spectrometry (LC-MS/MS)

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