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通过核磁共振研究水与大分子的相互作用:一种无正交的恒时方法及其在CI2中的应用。

Water-macromolecule interactions by NMR: a quadrature-free constant-time approach and its application to CI2.

作者信息

Melacini G, Boelens R, Kaptein R

机构信息

NMR Department, Bijvoet Center for Biomolecular Research, Utrecht University, The Netherlands.

出版信息

J Biomol NMR. 1999 Nov;15(3):189-201. doi: 10.1023/a:1008316612907.

Abstract

A pulse sequence is proposed to select water magnetization with enhanced specificity through a synergetic combination of several filtering principles. This approach relies on a constant-time evolution period implemented without quadrature detection, which results in a square root 2 increase in signal-to-noise ratios as compared to traditional non-selective methods for water filtration. In addition, the quadrature-free constant-time block facilitates the implementation of the water flip-back strategy, which leads to further gains in sensitivity. The proposed experiment was applied to unlabeled HEW lysozyme and to 15N-labeled chymotrypsin inhibitor 2 which was partially or non 13C-enriched. Water molecules belonging to a spine of hydration between two pseudo beta-sheet strands were identified, solving previously reported discrepancies between the X-ray and refined NMR structure of CI2. The proposed experiment in particularly suitable for hydration studies of mixtures of labeled and unlabeled components, such as ligand-macromolecule complexes.

摘要

提出了一种脉冲序列,通过几种滤波原理的协同组合来选择具有更高特异性的水磁化。该方法依赖于在不进行正交检测的情况下实现的恒时演化期,与传统的非选择性水过滤方法相比,这导致信噪比提高了根号2倍。此外,无正交恒时模块有助于水反转策略的实施,从而进一步提高灵敏度。所提出的实验应用于未标记的溶菌酶和部分或未进行13C富集的15N标记的胰凝乳蛋白酶抑制剂2。确定了属于两条假β-折叠链之间水合脊柱的水分子,解决了先前报道的CI2的X射线结构和精细NMR结构之间的差异。所提出的实验特别适用于标记和未标记成分混合物的水合研究,例如配体-大分子复合物。

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