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

• Published in: International journal of laboratory hematology Vol. 34; no. 3; pp. 232 - 236
• Main Authors: WARANG, P., KEDAR, P., GHOSH, K., COLAH, R.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-06-2012
• Subjects: 5'-Nucleotidase - blood; 5'-Nucleotidase - deficiency; Anemia, Hemolytic, Congenital - enzymology; Anemia, Hemolytic, Congenital - pathology; Ankyrins - deficiency; Case-Control Studies; ELISA reader; Enzyme-Linked Immunosorbent Assay - methods; Erythrocytes - chemistry; Erythrocytes - enzymology; hereditary non spherocytic hemolytic anemia; Humans; Jaundice, Obstructive - enzymology; Jaundice, Obstructive - pathology; Pyrimidine 5′ nucleotidase deficiency; Spherocytosis, Hereditary
• ISSN: 1751-5521; 1751-553X
• DOI: 10.1111/j.1751-553X.2011.01381.x

Summary
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.