Singh Kawarpal, Frydman Lucio
Department of Chemical and Biological Physics, Weizmann Institute of Science, 7610001 Rehovot, Israel.
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, CB2 1EW Cambridge, United Kingdom.
J Phys Chem Lett. 2024 May 30;15(21):5659-5664. doi: 10.1021/acs.jpclett.4c01190. Epub 2024 May 20.
Heteronuclear C-N couplings were measured in single-scan nuclear magnetic resonance (NMR) experiments for a variety of nitrogen-containing chemical compounds with varied structural characteristics, by using a one-dimensional (1D) C-N multiple-quantum (MQ)-filtered experiment. Sensitivity limitations of the MQ filtering were overcome by the combined use of N labeling and dissolution dynamic nuclear polarization (DNP), performed at cryogenic conditions and followed by quick and optimized sample melting and transfer procedures. Coupling information could thus be obtained from nucleotide bases, amino acids, urea, and aliphatic and aromatic amides, including the measurement of relatively small -couplings directly from the 1D filtered spectra. This experiment could pave the way for NMR-based analytical applications that investigate structural and stereochemical insights into nitrogen-containing compounds, including dipeptides and proteins, while relying on heteronuclear couplings and nuclear hyperpolarization.
通过一维(1D)碳-氮多量子(MQ)滤波实验,在单扫描核磁共振(NMR)实验中测量了各种具有不同结构特征的含氮化合物的异核碳-氮耦合。通过在低温条件下联合使用氮标记和溶解动态核极化(DNP),并随后进行快速且优化的样品熔化和转移程序,克服了MQ滤波的灵敏度限制。由此可以从核苷酸碱基、氨基酸、尿素以及脂肪族和芳香族酰胺中获得耦合信息,包括直接从1D滤波光谱测量相对较小的耦合。该实验可为基于NMR的分析应用铺平道路,这些应用依靠异核耦合和核超极化来研究含氮化合物(包括二肽和蛋白质)的结构和立体化学见解。