Department of Chemical and Biological Physics, Weizmann Institute of Science, 7610001, Rehovot, Israel.
Chemistry. 2022 Oct 18;28(58):e202201490. doi: 10.1002/chem.202201490. Epub 2022 Sep 26.
O and N are attractive targets for in vivo NMR spectroscopy and imaging, but low gyromagnetic ratios γ and fast spin relaxation complicate observations. This work explores indirect ways of detecting some of these sites with the help of proton-detected double resonance techniques. As standard coherence transfer methods are of limited use for such indirect detection, alternative routes for probing the quadrupolar spectra on H were tested. These centered on modulating the broadening effects imparted onto protons adjacent to the low-γ species through J couplings through either continuous wave or spin-echo double-resonance decoupling/recoupling sequences. As in all cases, the changes imparted by these double-resonance strategies were small due to the fast relaxation undergone by the quadrupoles, the sensitivity of these approaches was amplified by transferring their effects onto the abundant water H signal. These amplifications were mediated by the spontaneous exchanges that the labile Hs bound to O or N undergo with the water protons. In experiments designed on the basis of double-resonance spin echoes, these enhancements were imparted by looping the transverse encodings together with multiple longitudinal storage periods, leading to decoupling-recoupling with exchange (D-REX) sequences. In experiments designed on the basis of continuous on/off quadrupolar decoupling, these solvent exchanges were incorporated into chemical-exchange saturation transfer schemes, leading to decoupling-recoupling with saturation transfer (D-REST) sequences. Both of these variants harnessed sizable proportions of the easily detectable water signals, in order to characterize the NMR spectra and/or to image with atomic-site specificity the O and N species.
O 和 N 是体内 NMR 光谱和成像的有吸引力的目标,但低磁旋比γ和快速自旋弛豫使观察变得复杂。这项工作探索了借助质子探测双共振技术间接检测这些位点的方法。由于标准相干转移方法对于这种间接检测的用途有限,因此测试了探测 H 上的四极谱的替代途径。这些方法集中在调制通过 J 耦合施加到低γ物种相邻质子上的展宽效应上,无论是通过连续波还是自旋回波双共振去耦/再耦序列。在所有情况下,由于四极子经历的快速弛豫,这些双共振策略所赋予的变化都很小,这些方法的灵敏度通过将其效果转移到丰富的水 H 信号上来放大。这些放大是由与水质子发生自发交换的不稳定 Hs 与 O 或 N 结合所介导的。在基于双共振自旋回波设计的实验中,这些增强是通过将横向编码与多个纵向存储周期一起循环,从而导致带有交换的去耦-再耦(D-REX)序列来实现的。在基于连续开/关四极子去耦的实验中,这些溶剂交换被纳入化学交换饱和转移方案中,从而导致带有饱和转移的去耦-再耦(D-REST)序列。这两种变体都利用了易于检测的水信号的相当大的比例,以便对 NMR 光谱进行表征和/或对 O 和 N 物种进行具有原子位点特异性的成像。