Accelerating 15N and 13C R1 and R1ρ relaxation measurements by multiple pathway solid-state NMR experiments

被引:4
作者
Tognetti, Jacqueline [1 ,2 ]
Franks, W. Trent [1 ,2 ]
Gallo, Angelo [2 ]
Lewandowski, Jozef R. [2 ]
机构
[1] Univ Warwick, Dept Phys, Coventry CV4 7AL, W Midlands, England
[2] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
基金
英国生物技术与生命科学研究理事会; 欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
Solid-state NMR; Magic angle spinning; NMR relaxation; Staggered acquisition; DRIVEN SPIN-DIFFUSION; SIMULTANEOUS ACQUISITION; BACKBONE DYNAMICS; SENSITIVITY ENHANCEMENT; PARAMAGNETIC RELAXATION; PROTEIN; SPECTROSCOPY; ASSIGNMENT; SYSTEMS; H-1;
D O I
10.1016/j.jmr.2021.107049
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Magic angle spinning (MAS) Solid-state NMR is a powerful technique to probe dynamics of biological systems at atomic resolution. R-1 and R-1 rho relaxation measurements can provide detailed insight on amplitudes and time scales of motions, especially when information from several different site-specific types of probes is combined. However, such experiments are time-consuming to perform. Shortening the time necessary to record relaxation data for different nuclei will greatly enhance practicality of such approaches. Here, we present staggered acquisition experiments to acquire multiple relaxation experiments from a single excitation to reduce the overall experimental time. Our strategy enables one to collect N-15 and C-13 relaxation data in a single experiment in a fraction of the time necessary for two separate experiments, with the same signal to noise ratio. (C) 2021 The Authors. Published by Elsevier Inc.
引用
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页数:11
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