A systematic study of nucleotide analysis of human erythrocytes using an anionic exchanger and HPLC

A two-step procedure for rapid HPLC analysis of nucleotides from human erythrocytes is described. A strong anion exchanger Partisil-10 is used as column material. Elution of monophosphates requires about 12 min and the elution of di- and triphosphates 21 min. The elutions are performed separately and with different injections as such a procedure will save time otherwise used to re-condition the columns. In addition to the three adenylates other nucleotides such as GTP, GDP, IMP and NAD can be recorded as isolated, well-defined peaks, which can be subject to quantitative analysis. The mean value of ATP concentration for 12 healthy individuals was 1.55 +/- 0.05 mmol/l, about 25% higher than generally reported in the literature. Accurate estimates of ADP and AMP concentrations allowed calculation of mean values for the physiologically interesting ratios: adenylate energy charge (0.945 +/- 0.002) and equilibrium constant for adenylate kinase (1.205 +/- 0.053). GDP and GTP are present in concentrations that are about 4% of those for corresponding adenylates. The analysis of nucleotides in human erythrocytes is a useful way of studying erythrocyte preservation and investigating patients with hemolytic disorders.