Department of Chemistry, University of Colorado Denver, Denver, CO, USA.
Department of Mathematics, University of Colorado Denver, Denver, CO, USA.
Magn Reson Chem. 2021 Sep;59(9-10):853-863. doi: 10.1002/mrc.5114. Epub 2020 Nov 10.
We describe a new method for measuring molecular dynamics based on the deuterium solid-state nuclear magnetic resonance (NMR) quadrupolar order rotating frame relaxation rate R under static conditions. The observed quadrupolar order coherence is created using the broad-band Jeener-Broekaert excitation and is locked with a weak radio frequency (RF) field. We describe the experimental and theoretical approaches and show applications to a selectively deuterated valine side chain of the phosphorylated amyloid-β (1-40) fibrils phosphorylated at the serine-8 position. The R rate is sensitive to the rotameric exchange mode. For biological samples, the low spin-lock field in the 5- to 10-kHz range has the advantage of avoiding sample heating and dehydration. Thus, it provides an alternative to approaches based on single-quantum coherence, which require larger spin-lock fields.
我们描述了一种新的基于静态条件下氘固态核磁共振(NMR)四极核有序旋转框架弛豫率 R 的分子动力学测量方法。观察到的四极核有序相干是通过宽带 Jeener-Broekaert 激发产生的,并通过弱射频(RF)场锁定。我们描述了实验和理论方法,并展示了在选择性氘代缬氨酸侧链的磷酸化淀粉样β(1-40)纤维中丝氨酸-8 位磷酸化的应用。R 率对旋转异构体交换模式敏感。对于生物样品,5 至 10 kHz 范围内的低自旋锁定场具有避免样品加热和脱水的优点。因此,它为基于单量子相干的方法提供了替代方法,后者需要更大的自旋锁定场。