Key result
Zinc thiolate complexes are unreactive toward NO without dioxygen, but form S-nitrosothiols upon exposure to NO in air, NO2, or NOBF4, suggesting these species can liberate zinc from NOS.
NO cannot be the species directly responsible for S-nitrosothiol formation and loss of Zn2+ at the NOS dimer interface in vivo without the presence of dioxygen or other reactive nitrogen/oxygen species.
Zinc thiolate complexes containing N(2)S tridentate ligands were prepared to investigate their reactivity toward reactive nitrogen species, chemistry proposed to occur at the zinc tetracysteine thiolate site of nitric oxide synthase (NOS). The complexes are unreactive toward nitric oxide (NO) in the absence of dioxygen, strongly indicating that NO cannot be the species directly responsible for S-nitrosothiol formation and loss of Zn(2+) at the NOS dimer interface in vivo. S-Nitrosothiol formation does occur upon exposure of zinc thiolate solutions to NO in the presence of air, however, or to NO(2) or NOBF(4), indicating that these reactive nitrogen/oxygen species are capable of liberating zinc from the enzyme, possibly through generation of the S-nitrosothiol. Interaction between simple Zn(2+) salts and preformed S-nitrosothiols leads to decomposition of the -SNO moiety, resulting in release of gaseous NO and N(2)O. The potential biological relevance of this chemistry is discussed.
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Kozhukh et al. (2012) studied this question. Zinc thiolate complexes containing N(2)S tridentate ligands was evaluated on Reactivity toward reactive nitrogen species. Zinc thiolate complexes are unreactive toward NO without dioxygen, but form S-nitrosothiols upon exposure to NO in air, NO2, or NOBF4, suggesting these species can liberate zinc from NOS.
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