Kinetics study on recombinant alkaline phosphatase and correlation with the generated fluorescent signal

J Immunoassay Immunochem. 2018;39(1):108-118. doi: 10.1080/15321819.2017.1408022. Epub 2018 Jan 8.

Abstract

Alkaline phosphatase (AP) (EC 3.1.3.1) is one of the most commonly used enzymes in immunoassays. In VIDAS® assays (bioMérieux, Marcy l'Etoile, France), AP catalyzes the hydrolysis of 4-methylumbelliferyl phosphate (4-MUP) in 4-methylumbelliferone (4-MU) producing a fluorescent signal. This work introduces an original method of characterization of the kinetic parameters Km, Vmax, and Kcat of AP embedded in VIDAS® assays. Assessment of such constants allows us to predict the fluorescent signal generated for given amounts of enzyme and its associated substrate; in the particular case of VIDAS®, it has been estimated that 0.06 nmol/L of AP produces 3144 Relative Fluorescent Values (RFV).

Abbreviations: 4-MUP, 4-Methylumbelliferyl phosphate; 4-MU, 4-Methylumbelliferone; RFV, Relative Fluorescent Values; RFU, Relative Fluorescent Units; QDs, Quantum Dots; LoD, Limit of Detection.

Keywords: Michaelis-Menten regime; Turnover number; enzyme-based immunoassay; fluorescence; quantum dots.

MeSH terms

  • Alkaline Phosphatase / chemistry
  • Alkaline Phosphatase / metabolism*
  • Biocatalysis
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescence*
  • Hydrolysis
  • Hymecromone / analogs & derivatives
  • Hymecromone / chemistry
  • Hymecromone / metabolism
  • Kinetics
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism

Substances

  • Recombinant Proteins
  • 4-methylumbelliferyl phosphate
  • Hymecromone
  • Alkaline Phosphatase