Adducts
of catechols and histidine, which are produced by reactions of 1,2-quinones and p-quinone methides with histidyl residues in proteins incorporated into the insect exoskeleton, were characterized using electrospray ionization mass spectrometry (ESMS), tandem electrospray mass spectrometry (ESMS-MS, collision-induced dissociation), and ion trap mass spectrometry (ITMS). Compounds examined included adducts obtained from acid hydrolysates of Manduca sexta (tobacco hornworm) pupal cuticle exuviae and products obtained from model reactions under defined conditions. The ESMS and ITMS spectra of 6-(N-3)-histidyldopamine [6-(N-3)-His-DA, isomer] isolated from M. sexta cuticle were dominated by a [M ؉ H] ؉ ion at m/z 308, rather than the expected m/z 307. High-resolution fast atom bombardment MS yielded an empirical formula of C 14 H 18 N 3 O 5 , which was consistent with this compound being 6-(N-1)-histidyl-2-(3,4-dihydroxyphenyl)ethanol [6-(N-1)-His-DOPET] instead of a DA adduct. Similar results were obtained when histidyl-catechol compounds linked at C-7 of the catechol were examined; the (N-1) isomer was confirmed as a DA adduct, and the (N-3) isomer identified as an (N-1)-DOPET derivative. Direct MS analysis of unfractionated cuticle hydrolysate revealed intense parent and product ions characteristic of 6-and 7-linked adducts of histidine and DOPET. Mass spectrometric analysis of model adducts synthesized by electrochemical oxidative coupling of N-acetyldopamine (NADA) quinone and N-acetylhistidine (NAcH) identified the point of attachment in the two isomers. A prominent product ion corresponding to loss of CO 2 from [M ؉ H] ؉ of 2-NAcH-NADA confirmed this as being the (N-3) isomer. Loss of (H 2 O ؉ CO) from 6-NAcH-NADA suggested that this adduct was the (N-1) isomer. The results support the hypothesis that insect cuticle sclerotization involves the formation of C-N cross-links between histidine residues in cuticular proteins, and both ring and side-chain carbons of three catechols: NADA, N-alanyldopamine, and DOPET.