Department of Pharmacology and Center for Biomedical EPR Spectroscopy and Imaging, College of Medicine, The Ohio State University, Columbus, Ohio 43210, USA.
J Am Chem Soc. 2010 Dec 8;132(48):17157-73. doi: 10.1021/ja105198c. Epub 2010 Nov 11.
Nitrone spin traps have been employed as probes for the identification of transient radical species in chemical and biological systems using electron paramagnetic resonance (EPR) spectroscopy and have exhibited pharmacological activity against oxidative-stress-mediated diseases. Since superoxide radical anion (O2(•-)) is a major precursor to most reactive oxygen species and calix[4]pyrroles have been shown to exhibit high affinity to anions, a cyclic nitrone conjugate of calix[4]pyrrole (CalixMPO) was designed, synthesized, and characterized. Computational studies at the PCM/B3LYP/6-31+G(d,p)//B3LYP/6-31G(d) level suggest a pendant-type linkage between the calix[4]pyrrole and the nitrone to be the most efficient design for spin trapping of O2(•-), giving exoergic reaction enthalpies (ΔH(298K,aq)) and free energies (ΔG(298K,aq)) of -16.9 and -2.1 kcal/mol, respectively. (1)H NMR study revealed solvent-dependent conformational changes in CalixMPO leading to changes in the electronic properties of the nitronyl group upon H-bonding with the pyrrole groups as also confirmed by calculations. CalixMPO spin trapping of O2(•-) exhibited robust EPR spectra. Kinetic analysis of O2(•-) adduct formation and decay in polar aprotic solvents using UV-vis stopped-flow and EPR methods gave a larger trapping rate constant for CalixMPO and a longer half-life for its O2(•-) adduct compared to the commonly used nitrones. The unusually high reactivity of CalixMPO with O2(•-) was rationalized to be due to the synergy between the α-effect and electrostatic effect by the calix[4]pyrrole moiety on O2(•-) and the nitrone, respectively. This work demonstrates for the first time the application of an anion receptor for the detection of one of the most important radical intermediates in biological and chemical systems (i.e., O2(•-)).
氮氧自由基捕获剂已被用作电子顺磁共振(EPR)光谱法鉴定化学和生物系统中瞬态自由基的探针,并表现出对氧化应激介导疾病的药理活性。由于超氧自由基阴离子(O2(•-))是大多数活性氧物质的主要前体,而杯[4]吡咯已被证明对阴离子具有高亲和力,因此设计、合成并表征了杯[4]吡咯的环状硝酮共轭物(CalixMPO)。在 PCM/B3LYP/6-31+G(d,p)//B3LYP/6-31G(d)水平的计算研究表明,杯[4]吡咯和硝酮之间的悬垂型连接是 O2(•-)自旋捕获的最有效设计,分别给出-16.9 和-2.1 kcal/mol 的放热反应焓(ΔH(298K,aq))和自由能(ΔG(298K,aq))。(1)H NMR 研究表明,CalixMPO 存在溶剂依赖性构象变化,导致硝酮基团的电子性质在与吡咯基团形成氢键时发生变化,这也得到了计算的证实。CalixMPO 对 O2(•-)的自旋捕获显示出稳定的 EPR 光谱。使用紫外-可见停流和 EPR 方法在非质子极性溶剂中对 O2(•-)加合物的形成和衰减进行动力学分析,得到 CalixMPO 的较大捕获速率常数和其 O2(•-)加合物的较长半衰期,与常用的硝酮相比。CalixMPO 与 O2(•-)的异常高反应性可归因于杯[4]吡咯部分对 O2(•-)和硝酮的α效应和静电效应的协同作用。这项工作首次证明了阴离子受体在检测生物和化学系统中最重要的自由基中间体之一(即 O2(•-))中的应用。