Department of Chemistry, University of Michigan, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
J Am Chem Soc. 2012 Apr 11;134(14):6191-203. doi: 10.1021/ja210510g. Epub 2012 Mar 28.
An important factor that defines the toxicity of elements such as cadmium(II), mercury(II), and lead(II) with biological macromolecules is metal ion exchange dynamics. Intriguingly, little is known about the fundamental rates and mechanisms of metal ion exchange into proteins, especially helical bundles. Herein, we investigate the exchange kinetics of Cd(II) using de novo designed three-stranded coiled-coil peptides that contain metal complexing cysteine thiolates as a model for the incorporation of this ion into trimeric, parallel coiled coils. Peptides were designed containing both a single Cd(II) binding site, GrandL12AL16C [Grand = AcG-(LKALEEK)(5)-GNH(2)], GrandL26AL30C, and GrandL26AE28QL30C, as well as GrandL12AL16CL26AL30C with two Cd(II) binding sites. The binding of Cd(II) to any of these sites is of high affinity (K(A) > 3 × 10(7) M(-1)). Using (113)Cd NMR spectroscopy, Cd(II) binding to these designed peptides was monitored. While the Cd(II) binding is in extreme slow exchange regime without showing any chemical shift changes, incremental line broadening for the bound (113)Cd(II) signal is observed when excess (113)Cd(II) is titrated into the peptides. Most dramatically, for one site, L26AL30C, all (113)Cd(II) NMR signals disappear once a 1.7:1 ratio of Cd(II)/(peptide)(3) is reached. The observed processes are not compatible with a simple "free-bound" two-site exchange kinetics at any time regime. The experimental results can, however, be simulated in detail with a multisite binding model, which features additional Cd(II) binding site(s) which, once occupied, perturb the primary binding site. This model is expanded into differential equations for five-site NMR chemical exchange. The numerical integration of these equations exhibits progressive loss of the primary site NMR signal without a chemical shift change and with limited line broadening, in good agreement with the observed experimental data. The mathematical model is interpreted in molecular terms as representing binding of excess Cd(II) to surface Glu residues located at the helical interfaces. In the absence of Cd(II), the Glu residues stabilize the three-helical structure though salt bridge interactions with surface Lys residues. We hypothesize that Cd(II) interferes with these surface ion pairs, destabilizing the helical structure, and perturbing the primary Cd(II) binding site. This hypothesis is supported by the observation that the Cd(II)-excess line broadening is attenuated in GrandL26AE28QL30C, where a surface Glu(28), close to the metal binding site, was changed to Gln. The external binding site may function as an entry pathway for Cd(II) to find its internal binding site following a molecular rearrangement which may serve as a basis for our understanding of metal complexation, transport, and exchange in complex native systems containing α-helical bundles.
定义镉(II)、汞(II)和铅(II)等元素与生物大分子毒性的一个重要因素是金属离子交换动力学。有趣的是,对于金属离子进入蛋白质,特别是螺旋束的基本速率和机制,人们知之甚少。在此,我们使用从头设计的三股螺旋卷曲肽研究 Cd(II)的交换动力学,该肽含有作为将该离子掺入三聚体平行卷曲螺旋的金属络合半胱氨酸硫醇的模型。设计了包含单个 Cd(II)结合位点的肽,GrandL12AL16C [Grand = AcG-(LKALEEK)(5)-GNH(2)],GrandL26AL30C 和 GrandL26AE28QL30C,以及含有两个 Cd(II)结合位点的 GrandL12AL16CL26AL30C。这些位点与 Cd(II)的结合具有高亲和力(K(A) > 3 × 10(7) M(-1))。使用 (113)Cd NMR 光谱监测这些设计肽中 Cd(II)的结合情况。虽然 Cd(II)的结合处于极端缓慢交换状态,没有显示任何化学位移变化,但当向肽中滴定过量的 (113)Cd(II)时,观察到结合的 (113)Cd(II)信号的线宽逐渐增加。最显著的是,对于一个位点 L26AL30C,一旦达到 Cd(II)/(肽)(3)的 1.7:1 比,所有的 (113)Cd(II)NMR 信号都消失了。观察到的过程在任何时间范围内都与简单的“自由结合”双位点交换动力学不兼容。然而,实验结果可以通过具有附加 Cd(II)结合位点的多位点结合模型进行详细模拟,这些附加结合位点一旦被占据,就会干扰主要结合位点。该模型扩展为用于五位点 NMR 化学交换的微分方程。这些方程的数值积分表现出主要位点 NMR 信号的逐渐损失,而没有化学位移变化且线宽有限,与观察到的实验数据非常吻合。该数学模型从分子角度解释为代表位于螺旋界面处的过量 Cd(II)与表面 Glu 残基的结合。在没有 Cd(II)的情况下,通过与表面 Lys 残基的盐桥相互作用,Glu 残基稳定了三螺旋结构。我们假设 Cd(II)干扰这些表面离子对,破坏螺旋结构,并干扰主要的 Cd(II)结合位点。这一假设得到了以下观察结果的支持:在 GrandL26AE28QL30C 中,Cd(II)过量的线宽变窄得到了减弱,其中靠近金属结合位点的表面 Glu(28)被 Gln 取代。外部结合位点可能作为 Cd(II)进入其内部结合位点的入口途径,这可能是我们理解含有α-螺旋束的复杂天然系统中金属络合、运输和交换的基础。