Towards complete suppression of diagonal peaks in solid-state MAS NMR homonuclear chemical shift correlation spectra

IF 1.9 3区 化学 Q3 BIOCHEMICAL RESEARCH METHODS
Shengyu Zhang , Yuchen Li , Yansheng Ye , Fang Tian , Xinhua Peng , Riqiang Fu
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Abstract

The feasibility of applying the spin-echo based diagonal peak suppression method in solid-state MAS NMR homonuclear chemical shift correlation experiments is demonstrated. A complete phase cycling is designed to generate sine- and cosine-modulations of the chemical shift difference between the spin-diffused signals, enabling the quadrature detection in the indirect dimension. Meanwhile, all signals not involved in polarization transfer are refocused at the center of the indirect dimension. A data processing algorithm is developed to extract and suppress these spin-echo refocused signals without affecting nearby spin-diffused cross peaks. The processed spectrum is then converted into a conventional two-dimensional homonuclear chemical shift correlation spectrum, free of diagonal peaks. The effectiveness of this method is illustrated using a uniformly 13C-labeled Fmoc-leucine sample and a sample of human Atg8 homolog LC3B, directly conjugated to the amino headgroup of phosphatidylethanolamine (PE) lipids in liposomes.

Abstract Image

固态MAS核磁共振同核化学位移相关谱对角峰的完全抑制
论证了基于自旋回波对角峰抑制方法应用于固态MAS核磁共振同核化学位移相关实验的可行性。设计了一个完整的相位循环,以产生自旋扩散信号之间的化学位移差的正弦和余弦调制,从而实现间接维度的正交检测。同时,所有不参与极化转移的信号都被重新聚焦在间接维的中心。为了在不影响附近自旋扩散交叉峰的情况下提取和抑制这些自旋回波重聚焦信号,提出了一种数据处理算法。然后将处理后的光谱转换为传统的二维同核化学位移相关光谱,没有对角峰。使用统一的13c标记的fmoc -亮氨酸样品和人类at8同源物LC3B样品,直接偶联到脂质体中磷脂酰乙醇胺(PE)脂质的氨基头基,证明了该方法的有效性。
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来源期刊
CiteScore
3.80
自引率
13.60%
发文量
150
审稿时长
69 days
期刊介绍: The Journal of Magnetic Resonance presents original technical and scientific papers in all aspects of magnetic resonance, including nuclear magnetic resonance spectroscopy (NMR) of solids and liquids, electron spin/paramagnetic resonance (EPR), in vivo magnetic resonance imaging (MRI) and spectroscopy (MRS), nuclear quadrupole resonance (NQR) and magnetic resonance phenomena at nearly zero fields or in combination with optics. The Journal''s main aims include deepening the physical principles underlying all these spectroscopies, publishing significant theoretical and experimental results leading to spectral and spatial progress in these areas, and opening new MR-based applications in chemistry, biology and medicine. The Journal also seeks descriptions of novel apparatuses, new experimental protocols, and new procedures of data analysis and interpretation - including computational and quantum-mechanical methods - capable of advancing MR spectroscopy and imaging.
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