Backbone Torsion Angle Determination Using Proton Detected Magic-Angle Spinning Nuclear Magnetic Resonance

被引:3
|
作者
Xue, Kai [1 ]
Nimerovsky, Evgeny [1 ]
Movellan, Kumar A. Tekwani [1 ,2 ]
Becker, Stefan [1 ]
Andreas, Loren B. [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept NMR Based Struct Biol, D-37077 Gottingen, Germany
[2] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2022年 / 13卷 / 01期
关键词
SOLID-STATE NMR; PROTEIN BACKBONE; CHEMICAL-SHIFT; COUPLING-CONSTANTS; RF INHOMOGENEITY; GXXXG-LIKE; SPECTROSCOPY; PHI; RESOLUTION; PEPTIDES;
D O I
10.1021/acs.jpclett.1c03267
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Protein torsion angles define the backbone secondary structure of proteins. Magic-angle spinning (MAS) NMR methods using carbon detection have been developed to measure torsion angles by determining the relative orientation between two anisotropic interactions.dipolar coupling or chemical shift anisotropy. Here we report a new proton-detection based method to determine the backbone torsion angle by recoupling NH and CH dipolar couplings within the HCANH pulse sequence, for protonated or partly deuterated samples. We demonstrate the efficiency and precision of the method with microcrystalline chicken a spectrin SH3 protein and the influenza A matrix 2 (M2) membrane protein, using 55 or 90 kHz MAS. For M2, pseudo-4D data detect a turn between transmembrane and amphipathic helices.
引用
收藏
页码:18 / 24
页数:7
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