Laser-excited fluorescence spectroscopy was adopted for dityrosine det
ection in horse spleen apoferritin. Dityrosine was identified in horse
spleen apoferritin. Fractionation of acid-hydrolyzed horse spleen apo
ferritin showed fluorescence attributed to dityrosine, and other compo
unds, excited by 325-nm laser radiation. The other fluorescent compoun
ds resulted in a broad fluorescence emission spectrum of horse spleen
apoferritin. The broad emission band overlapped with the fluorescence
emission spectrum of pure dityrosine. Fractionation of horse spleen ap
oferritin acid hydrolysate prior to laser-excited fluorescence detecti
on was necessary for dityrosine quantitative analysis. The concentrati
on of dityrosine in horse spleen apoferritin was 2.5% (mol/mol), estim
ated from the method of standard addition.