Rapid and Convenient Oxidative Release of Thiol-Conjugated Forms of Microcystins for Chemical Analysis

摘要

Microcystins are potent cyclic heptapeptide toxins found in some cyanobacteria, and usually contain an alpha,beta-unsaturated carbonyl group that is readily conjugated to thiol-containing amino acids, peptides, and proteins in vivo and in vitro. Methods for deconjugating these types of adducts have recently been reported, but the reactions are slow or result in derivatized microcystins. Mercaptoethanol derivatives of a range of microtystins were therefore used as model compounds to develop deconjugation procedures in which the dialkyl sulfide. linkage was oxidized to a sulfoxide or sulfone that, when treated with-base, rapidly eliminated the adducted thiol as its sulfenate or sulfioate via beta-elimination to afford free microcystins with the alpha,beta-unsaturated carbonyl group intact These free microcystins can be analyzed by LC/MS to determine the toxin profile of bound microcystins: The method was tested on Cys- and GSH-derivatives of [Dha(7)]MC-LR. In solution, the deconjugation reactions were complete within minutes at pH 10:7 and: within, a few hours at pH 9.2, Oxidation of sulfides to sulfoxides is easier and more rapid than-Oxidation to sulfones, allowing the use of milder. oxidants and shorter reaction times. Oxidation of any methionine residues present in the microcystins occurs inevitably during these procedures, and interpretation of the microcystin profile obtained by LC/MS analysis needs to take this into account. Oxidation of tryptophan residues and degradation of microcystins by excess oxidant were circumvented by the addition of Me2SO as a sacrificial reducing agent These methods may be Useful for other compounds that undergo conjugation via thia-Michael addition, such as acrylamide and deoxynivalenol. Oxidationof sulfides to sulfoxides can occur in vivo and could affect the bioavailability of toxins and drugs conjugated via thia-Michael addition, potentially exacerbating oxidative stress by catalytically converting GSH to its sulfenate via conjugation, oxidation, and elimination to regenerate the free toxin.