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N-15 spin diffusion rate in solid-state NMR of totally enriched proteins: The magic angle spinning frequency effect

机译:完全富集蛋白质的固态NMR中N-15自旋扩散速率:幻角旋转频率效应

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摘要

As demonstrated by means of the one-dimensional solid-state MAS exchange experiment (CODEX), the rate of the proton driven spin diffusion between backbone N-15 nuclei in totally enriched protein depends strongly on the magic angle spinning (MAS) frequency: spin diffusion at MAS frequency 16 kHz is about 4-5 times slower as compared to that at MAS frequency I kHz which is due to the averaging of the homo- and hetero-nuclear dipolar interactions by MAS. It is important that even at the highest MAS frequencies used in our experiments the spin diffusion rate is comparable or larger than typical values of the spin-lattice relaxation rates of backbone nitrogens in solid proteins. Thus, the precise quantitative analysis of N-15 T-1's in totally enriched solid proteins may lead to wrong quantitative results. On the other hand, the effectiveness of the N-15-N-15 correlation and structure determination experiments making use of N-15-N-15 distances can be increased by decreasing the MAS frequency as far as possible, which is counter intuitive to the commonly applied fast MAS conditions in order to reduce the dipolar-broadened line widths for increased spectral resolution. (c) 2006 Elsevier Inc. All rights reserved.
机译:正如通过一维固态MAS交换实验(CODEX)所证明的那样,质子驱动自旋扩散在完全富集的蛋白质中的主链N-15核之间的扩散速率在很大程度上取决于幻角旋转(MAS)频率:自旋与MAS频率为1 kHz时相比,MAS频率为16 kHz时,扩散速度要慢4-5倍左右,这是由于MAS对同核和异核偶极相互作用的平均作用。重要的是,即使在我们实验中使用的最高MAS频率下,自旋扩散速率也要与固态蛋白质中主链氮的自旋晶格弛豫速率的典型值相当或更大。因此,对完全富集的固体蛋白中N-15 T-1的精确定量分析可能会导致错误的定量结果。另一方面,可以通过尽可能降低MAS频率来提高利用N-15-N-15距离进行N-15-N-15相关性和结构确定实验的效率,这与通常使用快速MAS条件以减小偶极展宽的线宽以提高光谱分辨率。 (c)2006 Elsevier Inc.保留所有权利。

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