Off-resonance 13C–2H REDOR NMR for site-resolved studies of molecular motion

IF 1.3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Martin D. Gelenter, Kelly J. Chen, Mei Hong
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引用次数: 2

Abstract

We introduce a 13C–2H Rotational Echo DOuble Resonance (REDOR) technique that uses the difference between on-resonance and off-resonance 2H irradiation to detect dynamic segments in deuterated molecules. By selectively inverting specific regions of the 2H magic-angle spinning (MAS) sideband manifold to recouple some of the deuterons to nearby carbons, we distinguish dynamic and rigid residues in 1D and 2D 13C spectra. We demonstrate this approach on deuterated GB1, H/D exchanged GB1, and perdeuterated bacterial cellulose. Numerical simulations reproduce the measured mixing-time and 2H carrier-frequency dependence of the REDOR dephasing of bacterial cellulose. Combining numerical simulations with experiments thus allow the extraction of motionally averaged quadrupolar couplings from REDOR dephasing values.

Abstract Image

非共振13C-2H REDOR核磁共振用于分子运动的位点分辨研究
我们介绍了一种13C-2H旋转回声双共振(REDOR)技术,该技术利用共振和非共振2H辐照的差异来检测氘化分子中的动态片段。通过选择性地反转2H魔角旋转(MAS)边带流形的特定区域,将一些氘核重新耦合到附近的碳上,我们在1D和2D 13C光谱中区分了动态残基和刚性残基。我们在氘化GB1、H/D交换GB1和渗透氘化细菌纤维素上证明了这种方法。数值模拟再现了测量的混合时间和2H载波频率对细菌纤维素的REDOR脱相的依赖。因此,将数值模拟与实验相结合,可以从REDOR消相值中提取运动平均四极耦合。
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来源期刊
Journal of Biomolecular NMR
Journal of Biomolecular NMR 生物-光谱学
CiteScore
6.00
自引率
3.70%
发文量
19
审稿时长
6-12 weeks
期刊介绍: The Journal of Biomolecular NMR provides a forum for publishing research on technical developments and innovative applications of nuclear magnetic resonance spectroscopy for the study of structure and dynamic properties of biopolymers in solution, liquid crystals, solids and mixed environments, e.g., attached to membranes. This may include: Three-dimensional structure determination of biological macromolecules (polypeptides/proteins, DNA, RNA, oligosaccharides) by NMR. New NMR techniques for studies of biological macromolecules. Novel approaches to computer-aided automated analysis of multidimensional NMR spectra. Computational methods for the structural interpretation of NMR data, including structure refinement. Comparisons of structures determined by NMR with those obtained by other methods, e.g. by diffraction techniques with protein single crystals. New techniques of sample preparation for NMR experiments (biosynthetic and chemical methods for isotope labeling, preparation of nutrients for biosynthetic isotope labeling, etc.). An NMR characterization of the products must be included.
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