Characterization of Products from the Reactions ofN-Acetyldopamine Quinone withN-Acetylhistidine

When insects harden or sclerotize their exoskeletons, quinones ofN-acetylated catecholamines such asN-acetyldopamine (NADA) undergo nucleophilic addition reactions with amino acids such as histidine in cuticular proteins. To determine the products that might form when this type of reaction occurs during cuticle sclerotization, the reactions between electrochemically prepared NADA quinone andN-acetylhistidine (NAcH), a protein model nucleophile, have been investigated at pH 7. Two major products, 6-[N-(N-acetylhistidyl)]-N-acetyldopamine and 2-[N-(N-acetylhistidyl)]-N-acetyldopamine, were purified by semipreparative reversed-phase liquid chromatography and identified by mass spectrometry and nuclear magnetic resonance spectroscopy. The relative molar ratio of the C(6) mono-addition adduct to the C(2) mono-addition adduct is 87:13. UV/vis spectroscopic analysis shows that both products have an absorption maximum at 284 nm. Cyclic voltammetry shows that these adducts are oxidized less readily than NADA.