Mazarguil H, Haran R, Laussac J P
Biochim Biophys Acta. 1982 Aug 27;717(3):465-72. doi: 10.1016/0304-4165(82)90289-6.
The binding of aluminium ion to [Leu5]-enkephalin has been investigated by 1H, 13C and 27Al NMR spectroscopy in dimethyl sulphoxide solution at different peptide/metal ratio. Analysis of the spectra suggests that Al3+ binds at two metal-binding sites. The binding of Al3+ at the first site involves the Tyr1CO, and Leu5COO- groups to give a 2:1 species in a tetracoordinated structure; whereas the binding of Al3+ at the second site utilizes the NH2 terminal groups of the tyrosine moiety in a 2:2 species. 27Al chemical shift values strongly suggest that the second type of aluminium atom displays an octahedral environment. On this basis, we discuss our data in terms of the coordination of aluminium with [Leu5]-enkephalin.
在不同肽/金属比例下,于二甲基亚砜溶液中通过1H、13C和27Al核磁共振光谱研究了铝离子与[亮氨酸5]-脑啡肽的结合。光谱分析表明,Al3+在两个金属结合位点结合。Al3+在第一个位点的结合涉及Tyr1CO和Leu5COO-基团,形成具有四面体结构的2:1物种;而Al3+在第二个位点的结合在2:2物种中利用了酪氨酸部分的NH2末端基团。27Al化学位移值强烈表明,第二种类型的铝原子呈现八面体环境。在此基础上,我们根据铝与[亮氨酸5]-脑啡肽的配位来讨论我们的数据。