Institut für Molekularbiologie und Biophysik, Eidgenössische Technische Hochschule Hönggerberg, CH-8093, Zürich, Switzerland.
J Biomol NMR. 1998 Aug;12(2):345-8. doi: 10.1023/A:1008268930690.
This paper describes the use of single transition-to-single transition polarization transfer (ST2-PT) in transverse relaxation-optimized spectroscopy (TROSY), where it affords a [Formula: see text] sensitivity enhancement for kinetically stable amide 15N-1H groups in proteins. Additional, conventional improvements of [15N,1H]-TROSY include that signal loss for kinetically labile 15N-1H groups due to saturation transfer from the solvent water is suppressed with the 'water flip back' technique and that the number of phase steps is reduced to two, which is attractive for the use of [15N,1H]-TROSY as an element in more complex NMR schemes. Finally, we show that the impact of the inclusion of the 15N steady-state magnetization (Pervushin et al., 1998) on the signal-to-noise ratio achieved with [15N,1H]-TROSY exceeds by up to two-fold the gain expected from the gyromagnetic ratios of 1H and 15N.
本文介绍了在横向弛豫优化波谱学(TROSY)中使用单转变到单转变极化转移(ST2-PT),这为动力学稳定的蛋白质酰胺 15N-1H 基团提供了[Formula: see text]的灵敏度增强。此外,常规的[15N,1H]-TROSY 改进包括通过“水翻转回”技术抑制溶剂水中的饱和转移导致动力学不稳定的 15N-1H 基团的信号损失,并且相步骤的数量减少到两个,这对于将[15N,1H]-TROSY 用作更复杂的 NMR 方案中的元素是有吸引力的。最后,我们表明,包含 15N 稳态磁化强度(Pervushin 等人,1998)对通过[15N,1H]-TROSY 获得的信噪比的影响超过了由于 1H 和 15N 的旋磁比而预期的增益的两倍。