A new simple approach for the determination of pyrimidine 5′-nucleotidase activity in human erythrocytes using an ELISA reader

摘要

Introduction: Pyrimidine 5′ nucleotidase type I (P5′N-1) deficiency is the most frequent abnormality of cell nucleotide metabolism causing hereditary non spherocytic hemolytic anemia (HNSHA). The aim of this study was to develop a simple method of determination of P5′N-1 activity in human erythrocytes using an ELISA reader Methods: Determination of P5′N-1 activity is based on the liberation of inorganic phosphorus (Pi) after incubation with uridine monophosphate/cytidine monophosphate. Inorganic phosphorus (Pi), a product of the enzymatic reaction is directly quantitated from its ultraviolet absorbance. Purine/Pyrimidine nucleotides ratio (OD 260: OD 280) was also measured Results: P5′N-1 deficient patients showed reduction in P5′N-1 activity (Mean±SD; 4.06±0.66 using an ELISA reader & 6.25±1.37 using a spectrophotometer) as compared to the normal control group (ELISA reader: 13.24±3.42 & Spectrophotometer: 18.25±3.20). Heterozygotes showed intermediate activity (ELISA reader: 6.06±0.48 & Spectrophotometer: 8.06±1.28), however they would have been missed on screening using the Purine/Pyrimidine nucleotides ratio Conclusion: Determination of P5′N-1 activity by using an ELISA reader is a new, simple, less time consuming and reliable method. It also avoids the use of radioactive material or HPLC which is a significant advantage.