Abstract
The effectiveness of eight thiol ligands for removing methylmercury (CH 3Hg(II)) from its glutathione and hemoglobin complexes in hemolyzed erythrocytes has been studied by 1H nuclear magnetic resonance spectroscopy. These complexes are the predominant methylmercury species in human erythrocytes. The effectiveness was determined from the exchange-averaged chemical shift of the resonance for the proton on the α-carbon of the cysteinyl residue and from the intensity of the resonance for the methylene protons of the glycine residue of reduced glutathione (GSH), both of which provide a measure of the amount of glutathione in the CH 3Hg(II)-complexed form. The thiol ligands were found to release GSH from its CH 3Hg(II) complex in the order 2, 3-dimercap-tosuccinic acid > mercaptosuccinic acid > cysteine > mercaptoacetic acid > D-penicillamine > 2, 3-dimercaptopropanesulfonic acid > N-acetyl-D,L-penicillamine > D.L-homocysteine.
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