Univ. Grenoble Alpes, CEA, CNRS, IRIG, MEM, 38000, Grenoble, France.
University of Iceland, Department of chemistry, Science Institute, Dunhaga 3, 107, Reykjavik, Iceland.
Angew Chem Int Ed Engl. 2022 Mar 14;61(12):e202114103. doi: 10.1002/anie.202114103. Epub 2022 Feb 1.
Efficiently hyperpolarizing proton-dense molecular solids through dynamic nuclear polarization (DNP) solid-state NMR is still an unmet challenge. Polarizing agents (PAs) developed so far do not perform well on proton-rich systems, such as organic microcrystals and biomolecular assemblies. Herein we introduce a new PA, cAsymPol-POK, and report outstanding hyperpolarization efficiency on 12.76 kDa U- C, N-labeled LecA protein and pharmaceutical drugs at high magnetic fields (up to 18.8 T) and fast magic angle spinning (MAS) frequencies (up to 40 kHz). The performance of cAsymPol-POK is rationalized by MAS-DNP simulations combined with electron paramagnetic resonance (EPR), density functional theory (DFT) and molecular dynamics (MD). This work shows that this new biradical is compatible with challenging biomolecular applications and unlocks the rapid acquisition of C- C and N- C correlations of pharmaceutical drugs at natural isotopic abundance, which are key experiments for structure determination.
通过动态核极化(DNP)固态 NMR 有效地极化质子丰富的分子固体仍然是一个未满足的挑战。迄今为止开发的极化剂(PAs)在质子丰富的系统(如有机微晶体和生物分子组装体)上的性能不佳。本文中,我们引入了一种新的 PA,cAsymPol-POK,并在高磁场(高达 18.8 T)和快速魔角旋转(MAS)频率(高达 40 kHz)下报告了在 12.76 kDa U-C、N 标记 LecA 蛋白和药物上的出色极化效率。通过与电子顺磁共振(EPR)、密度泛函理论(DFT)和分子动力学(MD)相结合的 MAS-DNP 模拟,对 cAsymPol-POK 的性能进行了合理化。这项工作表明,这种新的双自由基与具有挑战性的生物分子应用兼容,并能够快速获取药物的 C-C 和 N-C 相关,这是结构确定的关键实验。