Department of Biochemistry, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon.
J Biomol NMR. 1999 Jun;14(2):133-40. doi: 10.1023/A:1004583910874.
Recent studies have indicated that the relaxation rate of the (1)H-(13)C multiple-quantum coherence is much slower than that of the (1)H-(13)C single-quantum coherence for non-aromatic methine sites in (13) C labeled proteins and in nucleic acids at the slow tumbling limit. Several heteronuclear experiments have been designed to use a multiple-quantum coherence transfer scheme instead of the single-quantum transfer method, thereby increasing the sensitivity and resolution of the spectra. Here, we report a constant time, gradient and sensitivity enhanced HMQC experiment (CT-g/s-HMQC) and demonstrate that it has a significant sensitivity enhancement over constant time HMQC and constant time gradient and sensitivity enhanced HSQC experiments (CT-g/s-HSQC) when applied to a (13)C and (15) N labeled calmodulin sample in D(2)O. We also apply this approach to 3D NOESY-HMQC and doubly sensitivity enhanced TOCSY-HMQC experiments, and demonstrate that they are more sensitive than their HSQC counterparts.
最近的研究表明,在慢速转动极限下,(13)C 标记蛋白和核酸中非芳族亚甲位的(1)H-(13)C 多量子相干的弛豫率比(1)H-(13)C 单量子相干的弛豫率慢得多。已经设计了几种异核实验,以使用多量子相干转移方案代替单量子转移方法,从而提高光谱的灵敏度和分辨率。在这里,我们报告了一个恒时、梯度和灵敏度增强的 HMQC 实验(CT-g/s-HMQC),并证明当应用于 D(2)O 中的(13)C 和(15)N 标记钙调蛋白样品时,它比恒时 HMQC 和恒时梯度和灵敏度增强的 HSQC 实验(CT-g/s-HSQC)具有显著的灵敏度增强。我们还将这种方法应用于 3D NOESY-HMQC 和双重灵敏度增强的 TOCSY-HMQC 实验,并证明它们比它们的 HSQC 对应物更灵敏。