Selenium protection against mercury toxicity: high binding affinity of methylmercury by selenium-containing ligands in comparison with sulfur-containing ligands
1978; Elsevier BV; Volume: 9; Issue: 2 Linguagem: Inglês
10.1016/s0006-3061(00)80288-4
ISSN1873-3190
AutoresYukio Sugiura, Yoichi Tamai, Hisashi Tanaka,
Tópico(s)Selenium in Biological Systems
ResumoIn determining the protection of selenium against mercury toxicity, the binding affinity of methylmercury by various selenium-containing ligands was investigated by proton magnetic resonance (PMR) spectroscopy. The most striking feature was the small J199Hg-1H value of the selenocysteamine- and selenocysteine-methylmercury complexes, namely, the high affinity of the selenohydryl group to the mercury in comparison with those of the sulfhydryl and amino groups. The order of binding affinity of the coordination groups toward methylmercury is clearly SeH > SH ⩾ Se-Se > NH2 > S-S, SeCH3, SCH3. A definite correlation was found to exist between the mercury-proton coupling constants and the chemical shifts of methyl groups of the methylmercury complexes. A relationship betwen the order (Se > S > NH2) of affinity for methylmercury and the basicity (or electronegativity and covalent radius) of the donor groups was also discussed. These results suggest the high covalency of the CH3Hg-Se bond, which involves dπ-dπ back bonding.
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