IDENTIFICATION OF CYCLIC-NUCLEOTIDE DERIVATIVES SYNTHESIZED FOR RADIOIMMUNOASSAY DEVELOPMENT BY FAST-ATOM-BOMBARDMENT WITH COLLISION-INDUCED DISSOCIATION AND MASS-ANALYZED ION KINETIC-ENERGY SPECTROSCOPY
Rp. Newton et al., IDENTIFICATION OF CYCLIC-NUCLEOTIDE DERIVATIVES SYNTHESIZED FOR RADIOIMMUNOASSAY DEVELOPMENT BY FAST-ATOM-BOMBARDMENT WITH COLLISION-INDUCED DISSOCIATION AND MASS-ANALYZED ION KINETIC-ENERGY SPECTROSCOPY, Organic mass spectrometry, 28(8), 1993, pp. 899-906
The syntheses of 2'-O-succinyl, 2'-O-succinyltyrosinyl methyl ester an
d 2'-O-succinyliodotyrosinyl methyl ester derivatives of a cyclic nucl
eotide, derivatives necessary for the successful development of a spec
ific radioimmunoassay, are described. Fast atom bombardment with colli
sion-induced dissociation and mass-analysed ion kinetic energy spectro
scopy were used to verify the positions of substitution and the retent
ion of the 3',5'-cyclic phosphate moiety. Comparison of spectra produc
ed after different iodination times permitted the optimization of the
reaction conditions.