Bioinorganic Laboratory, Department of Chemistry, Indian Institute of Technology Bombay, Mumbai 400 076, India.
J Org Chem. 2010 May 21;75(10):3387-95. doi: 10.1021/jo1004247.
A new 1,3-diderivative of calix[4]arene appended with hydroxymethyl salicylyl imine has been synthesized and its ion recognition toward biologically relevant M(n+) ions studied. The receptor H(2)L showed selectivity toward Zn(2+) by switch-on fluorescence among the 12 metal ions studied with a detection limit of 192 ppb. The interaction of Zn(2+) with H(2)L has been further supported by absorption studies, and the stoichiometry of the complex formed (1:1) has been established on the basis of absorption and ESI MS. Competitive ion titrations carried out reveal that the Zn(2+) can be detected even in the presence of other metal ions of bioimportance. The mode of interaction of Zn(2+) with conjugate has been established by a fleet of computational calculations carried out in a cascade manner, either on the ligand or on the complex, wherein the final optimizations were carried out by the density functional theory (DFT) and found that the Zn(2+) and Cd(2+) indeed bind differently. In situ prepared [ZnL] complex responds to both inorganic phosphate as well as AMP, ADP, and ATP with a minimum detection limit of 426 ppb wherein the Zn(2+) from the complex is detached and recomplexed by the added phosphate moiety. It has been possible to build an INHIBIT logic gate for the conjugate using Zn(2+) and HPO(4)(2-) as inputs by monitoring the fluorescence emission band at 444 nm as output. The amino acid sensing abilities of [ZnL] have been explored by fluorescence and absorbance spectroscopy where it showed selectivity toward Cys, Asp, and His through the formation of the Zn(2+) complex of these amino acids by chelating through their side chain moieties. Thus, while H(2)L is selective for Zn(2+) among a number of cations, the [ZnL] is selective toward phosphate among a number of anions and also toward Asp, Cys, and His among the naturally occurring amino acids.
一种新的杯[4]芳烃 1,3-衍生物与羟甲基水杨酰亚胺相连,其对生物相关的 M(n+)离子的离子识别能力进行了研究。受体 H(2)L 在研究的 12 种金属离子中,通过荧光开关选择性地识别 Zn(2+),检测限为 192 ppb。吸收研究进一步支持了 Zn(2+)与 H(2)L 的相互作用,并根据吸收和 ESI MS 确定了形成的配合物的化学计量比(1:1)。进行的竞争性离子滴定表明,即使在存在其他生物重要金属离子的情况下,也可以检测到 Zn(2+)。通过级联方式进行的一系列计算计算,建立了 Zn(2+)与共轭物相互作用的模式,无论是在配体上还是在配合物上,最终优化都是通过密度泛函理论(DFT)进行的,并发现 Zn(2+)和 Cd(2+)确实以不同的方式结合。原位制备的[ZnL]配合物对无机磷酸盐以及 AMP、ADP 和 ATP 均有响应,检测限低至 426 ppb,其中配合物中的 Zn(2+)被添加的磷酸盐部分脱离并重新配位。通过监测 444nm 处的荧光发射带,使用 Zn(2+)和 HPO(4)(2-)作为输入,可以为该配合物构建一个 INHIBIT 逻辑门作为输出。通过荧光和吸收光谱研究了[ZnL]对氨基酸的传感能力,它通过与这些氨基酸的侧链部分螯合形成 Zn(2+)配合物,对 Cys、Asp 和 His 表现出选择性。因此,虽然 H(2)L 在多种阳离子中对 Zn(2+)具有选择性,但[ZnL]在多种阴离子中对磷酸盐具有选择性,在天然存在的氨基酸中对 Asp、Cys 和 His 也具有选择性。