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Optimized selection of slow-relaxing 13 C transitions in methyl groups of proteins: application to relaxation dispersion
Journal of Biomolecular NMR ( IF 2.7 ) Pub Date : 2020-10-01 , DOI: 10.1007/s10858-020-00349-3
Vitali Tugarinov 1 , Theodoros K Karamanos 1 , G Marius Clore 1
Affiliation  

Optimized selection of the slow-relaxing components of single-quantum 13C magnetization in 13CH3 methyl groups of proteins using acute (< 90°) angle 1H radio-frequency pulses, is described. The optimal selection scheme is more relaxation-tolerant and provides sensitivity gains in comparison to the experiment where the undesired (fast-relaxing) components of 13C magnetization are simply ‘filtered-out’ and only 90° 1H pulses are employed for magnetization transfer to and from 13C nuclei. When applied to methyl 13C single-quantum Carr-Purcell-Meiboom-Gill (CPMG) relaxation dispersion experiments for studies of chemical exchange, the selection of the slow-relaxing 13C transitions results in a significant decrease in intrinsic (exchange-free) transverse spin relaxation rates of all exchanging species. For exchanging systems involving high-molecular-weight species, the lower transverse relaxation rates translate into an increase in the information content of the resulting relaxation dispersion profiles.



中文翻译:

蛋白质甲基中慢弛豫 13 C 跃迁的优化选择:应用于弛豫分散

描述了使用锐角 (< 90°) 1 H 射频脉冲在蛋白质的13 CH 3甲基基团中优化选择单量子13 C 磁化的缓慢松弛成分。与实验相比,最佳选择方案具有更强的弛豫容忍度并提供灵敏度增益,实验中13 C 磁化的不需要(快速弛豫)成分被简单地“过滤掉”,并且仅采用 90° 1 H 脉冲进行磁化转移往返于13 C 原子核。当应用于甲基13用于化学交换研究的 C 单量子 Carr-Purcell-Meiboom-Gill (CPMG) 弛豫色散实验,缓慢弛豫13 C 跃迁的选择导致本征(无交换)横向自旋弛豫率的显着降低所有交换物种。对于涉及高分子量物质的交换系统,较低的横向弛豫率转化为所得弛豫色散分布的信息含量的增加。

更新日期:2020-10-02
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