Department of Chemistry, University of Michigan, Ann Arbor, MI, USA; Biophysics, Biomedical Engineering, Macromolecular Science and Engineering, University of Michigan, Ann Arbor, MI, USA.
Department of Chemistry, University of Michigan, Ann Arbor, MI, USA.
Solid State Nucl Magn Reson. 2019 Oct;102:36-46. doi: 10.1016/j.ssnmr.2019.07.002. Epub 2019 Jul 12.
NMR spectroscopy is a powerful experimental technique to study biological systems at the atomic resolution. However, its intrinsic low sensitivity results in long acquisition times that in extreme cases lasts for days (or even weeks) often exceeding the lifetime of the sample under investigation. Different paramagnetic agents have been used in an effort to decrease the spin-lattice (T) relaxation times of the studied nuclei, which are the main cause for long acquisition times necessary for signal averaging to enhance the signal-to-noise ratio of NMR spectra. Consequently, most of the experimental time is "wasted" in waiting for the magnetization to recover between successive scans. In this review, we discuss how to set up an optimal paramagnetic relaxation enhancement (PRE) system to effectively reduce the T relaxation times avoiding significant broadening of NMR signals. Additionally, we describe how PRE-agents can be used to provide structural and dynamic information and can even be used to follow the intermediates of chemical reactions and to speed-up data acquisition. We also describe the unique challenges and benefits associated with the application of PRE to solid-state NMR spectroscopy, explaining how the use of PREs is more complex for membrane mimetic systems as PREs can also be exploited to change the alignment of oriented membrane systems. Functionalization of membrane mimetics, such as bicelles, can provide a controlled region of paramagnetic effect that has the potential, together with the desired alignment, to provide crucial biologically relevant structural information. And finally, we discuss how paramagnetic metals can be utilized to further increase the dynamic nuclear polarization (DNP) effects and how to preserve the enhancements when dissolution DNP is implemented.
NMR 光谱学是一种强大的实验技术,可用于在原子分辨率下研究生物系统。然而,其固有低灵敏度导致采集时间长,在极端情况下,采集时间可持续数天(甚至数周),通常超过研究样品的寿命。为了降低研究核自旋晶格(T1)弛豫时间,已经使用了不同的顺磁试剂,这是需要进行信号平均以提高 NMR 光谱信噪比所必需的长采集时间的主要原因。因此,大部分实验时间都“浪费”在等待磁化在连续扫描之间恢复。在这篇综述中,我们讨论了如何建立最佳的顺磁弛豫增强(PRE)系统,以有效地缩短 T1 弛豫时间,同时避免 NMR 信号的显著展宽。此外,我们还描述了 PRE 试剂如何用于提供结构和动态信息,甚至可用于跟踪化学反应的中间产物并加快数据采集。我们还描述了将 PRE 应用于固态 NMR 光谱学所带来的独特挑战和好处,解释了 PRE 对于模拟膜系统的应用为何更为复杂,因为 PRE 还可以用于改变取向膜系统的排列。膜类似物的功能化,如双胶束,可以提供一个可控的顺磁效应区域,该区域与所需的取向一起,有可能提供关键的、与生物学相关的结构信息。最后,我们讨论了如何利用顺磁金属进一步提高动态核极化(DNP)效应,以及在实施溶解 DNP 时如何保持增强效果。