LC-MS/MS multiplexed assay for the quantitation of a therapeutic protein BMS-986089 and the target protein Myostatin

Bioanalysis. 2016 Feb;8(3):193-204. doi: 10.4155/bio.15.238. Epub 2016 Jan 26.

Abstract

Background: Therapeutic protein discovery study highlights the need for the development of quantitative bioanalytical methods for determining the levels of both the therapeutic protein and the target protein, as well.

Results: For the quantitation of BMS-986089, both accuracy (99-103%) and precision (2.4-12%) were obtained for the analysis of the surrogate peptide (ITYGGNSPVQEFTVPGR), in addition to the accuracy (100-108%) and precision (0.7-18%) that were obtained for the analysis of the surrogate peptide (VVSVLTVLHQDWLNGK). For Myostatin, accuracy (94-103%) and precision (2.4-14.9%) were obtained for the analysis of the surrogate peptide (IPAMVVDR).

Conclusion: The developed method was applied to the analysis of samples following dosing of BMS-986089 to mice. This method highlights the potential of LC-MS/MS-based methods to eventually assess in vivo drug-target engagement.

Keywords: LC–MS/MS-based multiplexed detection; surrogate peptides; target protein; therapeutic protein.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Chromatography, Liquid / economics
  • Chromatography, Liquid / methods*
  • Cost-Benefit Analysis
  • Humans
  • Immunoglobulin G / analysis
  • Immunoglobulin G / metabolism
  • Immunoglobulin G / pharmacology
  • Immunoglobulin G / therapeutic use
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Myostatin / analysis*
  • Myostatin / metabolism
  • Peptide Fragments / analysis
  • Peptide Fragments / chemistry
  • Rats
  • Recombinant Fusion Proteins / analysis*
  • Recombinant Fusion Proteins / pharmacokinetics
  • Recombinant Fusion Proteins / pharmacology
  • Recombinant Fusion Proteins / therapeutic use
  • Tandem Mass Spectrometry / economics
  • Tandem Mass Spectrometry / methods*
  • Trypsin / metabolism

Substances

  • Immunoglobulin G
  • Myostatin
  • Peptide Fragments
  • Recombinant Fusion Proteins
  • Trypsin