Lutz Patricia B, Bayse Craig A
Department of Science, Technology and Mathematics, Regent University, Virginia Beach, Virginia 23464, United States.
Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, Virginia 23529, United States.
J Inorg Biochem. 2016 Apr;157:94-103. doi: 10.1016/j.jinorgbio.2016.01.013. Epub 2016 Jan 12.
Reducible sulfur and selenium (r-S/Se) compounds, defined as sulfur and selenium compounds not in the lowest -2 oxidation state (e.g., -1 to +6), release Zn(2+) from zinc-sulfur proteins such as zinc fingers (ZFs) and metallothionein. A series of density functional theory calculations was performed on donor-acceptor complexes between r-S/Se compounds and models of the Cys2His2, Cys3His and Cys4 ZF sites. These S⋯S/Se chalcogen bonding interactions consist of the donation of electron density from a S lone pair on the ZF model to a S/Se-X antibonding molecular orbital of the r-S/Se compound. The strength of the interaction was shown to be dependent upon the Lewis basicity of the ZF model (Cys4>Cys3His>Cys2His2) and the Lewis acidity of the r-S/Se compound as measured by the energy of the S/Se-X antibonding orbital. Interactions with the softer r-Se compounds were stronger than the r-S compounds, consistent with the greater reactivity of the former with ZF proteins.
可还原硫和硒(r-S/Se)化合物定义为硫和硒的化合物,其氧化态并非最低的-2价(例如,从-1到+6价),这类化合物可从锌硫蛋白如锌指(ZFs)和金属硫蛋白中释放出Zn(2+)。对r-S/Se化合物与Cys2His2、Cys3His和Cys4锌指位点模型之间的供体-受体复合物进行了一系列密度泛函理论计算。这些S⋯S/Se硫族键相互作用包括从锌指模型上的硫孤对电子向r-S/Se化合物的S/Se-X反键分子轨道的电子密度捐赠。相互作用的强度显示取决于锌指模型的路易斯碱度(Cys4>Cys3His>Cys2His2)以及通过S/Se-X反键轨道能量测量的r-S/Se化合物的路易斯酸度。与较软的r-Se化合物的相互作用强于r-S化合物,这与前者与锌指蛋白的反应活性更高相一致。