快速 MAS 固态 NMR 下自旋-1/2 和半整数四极核之间的高分辨率异核相关性

IF 3.3 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Manoj Kumar Pandey , Yusuke Nishiyama
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引用次数: 0

摘要

高各向同性分辨率对于阐明具有多个位点的样品结构至关重要。在本研究中,我们利用基于 TRAPDOR 的异核多重量子相干(T-HMQC)和一对基于对称-分裂-t1 多量子魔角旋转(MQMAS)的长余弦振幅调制低功率(cos-lp)脉冲的优势、我们在快速 MAS(70 kHz)条件下开发了质子探测二维 35Cl/1H T-HMQC-MQMAS 脉冲序列,以实现通过质子连接的自旋-3/2(35Cl)原子核间接维度的高分辨率。由于 T-HMQC 不仅能极化单量子中心转变(SQCT),还能极化三量子(TQ)相干,因此建议的二维脉冲序列是通过选择两种相干途径(SQCT →TQ →SQCT 和 TQ → SQCT →TQ)来实现的,从而得到 35Cl 的各向同性维度,在分辨率方面优于现有的双量子卫星转变(DQST)T-HMQC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-resolution heteronuclear correlations between spin-1/2 and half-integer quadrupolar nuclei under fast MAS solid-state NMR

High-resolution heteronuclear correlations between spin-1/2 and half-integer quadrupolar nuclei under fast MAS solid-state NMR

High isotropic resolution is essential for the structural elucidation of samples with multiple sites. In this study, utilizing the benefits of TRAPDOR-based heteronuclear multiple quantum coherence (T-HMQC) and a pair of one rotor period long cosine amplitude modulated low-power (cos-lp) pulse-based symmetric-split-t1 multiple-quantum magic angle spinning (MQMAS) methods, we have developed a proton-detected 2D 35Cl/1H T-HMQC-MQMAS pulse sequence under fast MAS (70 kHz) to achieve high-resolution in the indirect dimension of the spin-3/2 (35Cl) nuclei connected via protons. As T-HMQC polarizes not only single-quantum central transition (SQCT) but also triple-quantum (TQ) coherences, the proposed 2D pulse sequence is implemented via selection of two coherence pathways (SQCT TQ SQCT and TQ SQCT TQ) resulting in the 35Cl isotropic dimension and is superior to the existing double-quantum satellite-transition (DQST) T-HMQC in terms of resolution.

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来源期刊
Biophysical chemistry
Biophysical chemistry 生物-生化与分子生物学
CiteScore
6.10
自引率
10.50%
发文量
121
审稿时长
20 days
期刊介绍: Biophysical Chemistry publishes original work and reviews in the areas of chemistry and physics directly impacting biological phenomena. Quantitative analysis of the properties of biological macromolecules, biologically active molecules, macromolecular assemblies and cell components in terms of kinetics, thermodynamics, spatio-temporal organization, NMR and X-ray structural biology, as well as single-molecule detection represent a major focus of the journal. Theoretical and computational treatments of biomacromolecular systems, macromolecular interactions, regulatory control and systems biology are also of interest to the journal.
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