主链酰胺氘化引起的二键、三键和四键同位素移位的核磁共振检测和构象依赖性

IF 1.3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biomolecular NMR Pub Date : 2023-04-24 DOI:10.1007/s10858-023-00414-7
Andrei T. Alexandrescu, Aurelio J. Dregni, Carolyn M. Teschke
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引用次数: 0

摘要

当附近的原子是不同的同位素时,由于核屏蔽的微小差异而发生核磁共振同位素移位。对于溶解在1:1 H2O:D2O中的分子,所产生的N-H和N-D同位素的混合物导致相邻原子核的共振发生小的分裂。我们使用多维核磁共振来测量蛋白质CUS-3iD和CspA的同位素位移。在高分辨率二维15N-TROSY实验中,我们观察到四键4∆N(ND)同位素位移与扭转角psi相关。在H(N)CO光谱中检测到的三键3∆C′(ND)同位素位移与残留内H- o距离相关,与二面角phi的相关性较小。同位素位移的构象依赖性与先前文献报道的一致。4∆N(ND)和3∆C’(ND)同位素位移对引起同位素位移的原子之间的距离和经历分裂的原子之间的距离都很敏感,然而,这些距离与主二面角密切相关,因此很难通过立体化学对同位素位移的贡献来解决距离问题。H(NCA)CO光谱用于测量双键2∆C′(ND)同位素位移和[D]/[H]分馏因子。在25°温度范围内,这两个参数对氢键位点没有显著差异,表明它们对氢键不敏感。最后,利用H(CA)CO光谱中2∆C′(ND)和3∆C′(ND)同位素移位组合产生的四重调,测量了蛋白质cu - 3id中相邻序列A315-S316的同步氢交换。在我们的许多实验中,我们观察到由于样品氘锁使用10% D2O而产生的轻微共振,这表明同位素位移可能是标准核磁共振实验中光谱异质性的来源。我们认为同位素转移的应用,如构象分析和相关氢交换可以受益于更大的磁场变得可用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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NMR detection and conformational dependence of two, three, and four-bond isotope shifts due to deuteration of backbone amides

NMR isotope shifts occur due to small differences in nuclear shielding when nearby atoms are different isotopes. For molecules dissolved in 1:1 H2O:D2O, the resulting mixture of N-H and N-D isotopes leads to a small splitting of resonances from adjacent nuclei. We used multidimensional NMR to measure isotope shifts for the proteins CUS-3iD and CspA. We observed four-bond 4∆N(ND) isotope shifts in high-resolution 2D 15N-TROSY experiments of the perdeuterated proteins that correlate with the torsional angle psi. Three-bond 3∆C’(ND) isotope shifts detected in H(N)CO spectra correlate with the intraresidue H-O distance, and to a lesser extent with the dihedral angle phi. The conformational dependence of the isotope shifts agree with those previously reported in the literature. Both the 4∆N(ND) and 3∆C’(ND) isotope shifts are sensitive to distances between the atoms giving rise to the isotope shifts and the atoms experiencing the splitting, however, these distances are strongly correlated with backbone dihedral angles making it difficult to resolve distance from stereochemical contributions to the isotope shift. H(NCA)CO spectra were used to measure two-bond 2∆C’(ND) isotope shifts and [D]/[H] fractionation factors. Neither parameter showed significant differences for hydrogen-bonded sites, or changes over a 25° temperature range, suggesting they are not sensitive to hydrogen bonding. Finally, the quartet that arises from the combination of 2∆C’(ND) and 3∆C’(ND) isotope shifts in H(CA)CO spectra was used to measure synchronized hydrogen exchange for the sequence neighbors A315-S316 in the protein CUS-3iD. In many of our experiments we observed minor resonances due to the 10% D2O used for the sample deuterium lock, indicating isotope shifts can be a source of spectral heterogeneity in standard NMR experiments. We suggest that applications of isotope shifts such as conformational analysis and correlated hydrogen exchange could benefit from the larger magnetic fields becoming available.

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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.
期刊最新文献
Pitfalls in measurements of R1 relaxation rates of protein backbone 15N nuclei. Towards cost-effective side-chain isotope labelling of proteins expressed in human cells. Optimising in-cell NMR acquisition for nucleic acids. Transverse relaxation optimized spectroscopy of NH2 groups in glutamine and asparagine side chains of proteins. Micromolar fluoride contamination arising from glass NMR tubes and a simple solution for biomolecular applications
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