Yau Wai-Ming, Thurber Kent R, Tycko Robert
Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0520, United States.
Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0520, United States.
J Magn Reson. 2014 Jul;244:98-106. doi: 10.1016/j.jmr.2014.05.002. Epub 2014 May 20.
We describe the synthesis of new nitroxide-based biradical, triradical, and tetraradical compounds and the evaluation of their performance as paramagnetic dopants in dynamic nuclear polarization (DNP) experiments in solid state nuclear magnetic resonance (NMR) spectroscopy with magic-angle spinning (MAS). Under our experimental conditions, which include temperatures in the 25-30 K range, a 9.4 T magnetic field, MAS frequencies of 6.2-6.8 kHz, and microwave irradiation at 264.0 GHz from a 800 mW extended interaction oscillator source, the most effective compounds are triradicals that are related to the previously-described compound DOTOPA-TEMPO (see Thurber et al., 2010), but have improved solubility in glycerol/water solvent near neutral pH. Using these compounds at 30 mM total nitroxide concentration, we observe DNP enhancement factors of 92-128 for cross-polarized (13)C NMR signals from (15)N,(13)C-labeled melittin in partially protonated glycerol/water, and build-up times of 2.6-3.8s for (1)H spin polarizations. Net sensitivity enhancements with biradical and tetraradical dopants, taking into account absolute (13)C NMR signal amplitudes and build-up times, are approximately 2-4 times lower than with the best triradicals.
我们描述了新型基于氮氧化物的双自由基、三自由基和四自由基化合物的合成,以及在具有魔角旋转(MAS)的固态核磁共振(NMR)光谱的动态核极化(DNP)实验中对其作为顺磁掺杂剂性能的评估。在我们的实验条件下,包括25 - 30 K范围内的温度、9.4 T的磁场、6.2 - 6.8 kHz的MAS频率以及来自800 mW扩展相互作用振荡器源的264.0 GHz微波辐射,最有效的化合物是与先前描述的化合物DOTOPA - TEMPO相关的三自由基(见Thurber等人,2010年),但在接近中性pH值的甘油/水溶剂中具有更好的溶解性。在总氮氧化物浓度为30 mM的情况下使用这些化合物,我们观察到在部分质子化的甘油/水中,来自(15)N、(13)C标记的蜂毒肽交叉极化(13)C NMR信号的DNP增强因子为92 - 128,以及(1)H自旋极化的建立时间为2.6 - 3.8秒。考虑到绝对(13)C NMR信号幅度和建立时间,双自由基和四自由基掺杂剂的净灵敏度增强比最佳三自由基低约2 - 4倍。