Abstract
A sensitive method to directly measure the mass of inositol phosphates from biologic samples is described. The procedure uses ammonium sulfate gradient elution anion exchange column chromatography to isolate inositol monophosphate, bisphosphate, trisphosphate, and tetrakisphosphate. The isolated fractions are dephosphorylated and subsequently desalted by a novel approach using solid barium hydroxide in a 1:1 stoichiometric ratio to the amount of ammonium sulfate present in the dephosphorylated sample. The myo-inositol derived from each inositol phosphate species was quantified by stable isotope dilution gas chromatography-mass spectrometry of the hexakis(trimethylsilyl) derivative using hexadeutero-myo-inositol as the internal standard. The applicability and sensitivity of this method are illustrated by measuring the mass of individual inositol phosphates in isolated adult canine cardiac myocytes.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1925-1934 |
| Number of pages | 10 |
| Journal | Journal of Lipid Research |
| Volume | 31 |
| Issue number | 10 |
| State | Published - 1990 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Endocrinology
- Cell Biology