Chemical research in toxicology | Vol.8, Issue.3 | | Pages 414-21
Alkylation of oxytocin by S-(2-chloroethyl)glutathione and characterization of adducts by tandem mass spectrometry and Edman degradation.
S-(2-Chloroethyl)glutathione (CEG), an alkylating agent formed by glutathione conjugation with 1,2-dichloroethane (DCE), is able to alkylate DNA and proteins. As a prelude to identification of specific protein alkylation sites, the peptide oxytocin was alkylated by CEG, and tandem mass spectrometry was used to identify the alkylation sites. It was found that mono-, bis-, and tris-adducts can result from alkylation of reduced oxytocin and that tandem mass spectrometry differentiated (S-[2-(Cys1)ethyl]glutathione)oxytocin (mono-adduct Cys-1) from (S-[2-(Cys1,6)ethyl]glutathione)oxytocin (mono-adduct Cys-6). Manual Edman degradation was used to eliminate the possibility that alkylation has occurred at Tyr-2 rather than at Cys-1 in the case of (S-[2-(Cys1,6)ethyl]glutathione)oxytocin (bis-adduct) and mono-adduct Cys-1. A mono-adduct homodimer resulting from alkylation at Cys-6 and disulfide bridge formation through Cys-1 was also identified. Oxidized oxytocin formed two minor adducts, representing less than 5% of the oxytocin present in the reaction mixture. These findings demonstrate that alkylation of oxytocin by the episulfonium ion of CEG did occur, as evidenced by tandem mass spectrometry, and that characterization of these adducts will aid in the identification of alkylated amino acids in proteins exposed to CEG.
Original Text (This is the original text for your reference.)
Alkylation of oxytocin by S-(2-chloroethyl)glutathione and characterization of adducts by tandem mass spectrometry and Edman degradation.
S-(2-Chloroethyl)glutathione (CEG), an alkylating agent formed by glutathione conjugation with 1,2-dichloroethane (DCE), is able to alkylate DNA and proteins. As a prelude to identification of specific protein alkylation sites, the peptide oxytocin was alkylated by CEG, and tandem mass spectrometry was used to identify the alkylation sites. It was found that mono-, bis-, and tris-adducts can result from alkylation of reduced oxytocin and that tandem mass spectrometry differentiated (S-[2-(Cys1)ethyl]glutathione)oxytocin (mono-adduct Cys-1) from (S-[2-(Cys1,6)ethyl]glutathione)oxytocin (mono-adduct Cys-6). Manual Edman degradation was used to eliminate the possibility that alkylation has occurred at Tyr-2 rather than at Cys-1 in the case of (S-[2-(Cys1,6)ethyl]glutathione)oxytocin (bis-adduct) and mono-adduct Cys-1. A mono-adduct homodimer resulting from alkylation at Cys-6 and disulfide bridge formation through Cys-1 was also identified. Oxidized oxytocin formed two minor adducts, representing less than 5% of the oxytocin present in the reaction mixture. These findings demonstrate that alkylation of oxytocin by the episulfonium ion of CEG did occur, as evidenced by tandem mass spectrometry, and that characterization of these adducts will aid in the identification of alkylated amino acids in proteins exposed to CEG.
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