An enzyme-linked immunosorbent assay for the rapid quantification of intracellular and extracellular guanosine 3',5'-cyclic monophosphate in cultured glial cells

Neurochem Res. 2004 Nov;29(11):2177-87. doi: 10.1007/s11064-004-8675-x.

Abstract

A sensitive enzyme-linked, indirect immunosorbent assay (ELISA) for the determination of guanosine 3',5'-cyclic monophosphate (cGMP) in glial cells is described. The assay uses an antiserum produced against succinylated cGMP and is based on the competition between endogenous cGMP and a fixed amount of immobilized antigen. The antibody exhibited a high degree of specificity with negligible cross reactivity with other nucleotides or related compounds. The standard curve, linearized using a logit-log transformation, had an operating range of 1 fmol/50 microl to 5 pmol/50 microl. The sensitivity of the assay was significantly increased by acetylation of standards and samples. Recoveries of cGMP from samples of cultured cells ranged from 85% to 105% with a mean recovery of 97% +/- 7%. Levels of cGMP measured with the ELISA were in agreement with the corresponding values obtained using radioimmunoassay. The present method provides for a cheap, sensitive and simple alternative to the commercially available cGMP assays.

MeSH terms

  • Alkaline Phosphatase / chemistry
  • Animals
  • Antibody Specificity
  • Antigens / chemistry
  • Calibration
  • Cells, Cultured
  • Cross Reactions
  • Cyclic GMP / analysis*
  • Cyclic GMP / biosynthesis
  • Cyclic GMP / immunology
  • Enzyme-Linked Immunosorbent Assay / methods*
  • Indicators and Reagents
  • Neuroglia / chemistry*
  • Neuroglia / metabolism
  • Rabbits / immunology
  • Radioimmunoassay
  • Reference Standards
  • Reproducibility of Results

Substances

  • Antigens
  • Indicators and Reagents
  • Alkaline Phosphatase
  • Cyclic GMP