Lundström Patrik, Vallurupalli Pramodh, Religa Tomasz L, Dahlquist Frederick W, Kay Lewis E
Department of Medical Genetics, The University of Toronto, Toronto, ON, Canada, M5S 1A8.
J Biomol NMR. 2007 May;38(1):79-88. doi: 10.1007/s10858-007-9149-7. Epub 2007 Apr 27.
A pulse sequence is described for recording single-quantum (13)C-methyl relaxation dispersion profiles of (13)C-selectively labeled methyl groups in proteins that offers significant improvements in sensitivity relative to existing approaches where initial magnetization derives from (13)C polarization. Sensitivity gains in the new experiment are achieved by making use of polarization from (1)H spins and (1)H --> (13)C --> (1)H type magnetization transfers. Its utility has been established by applications involving three different protein systems ranging in molecular weight from 8 to 28 kDa, produced using a number of different selective labeling approaches. In all cases exchange parameters from both (13)C-->(1)H and (1)H --> (13)C --> (1)H classes of experiment are in good agreement, with gains in sensitivity of between 1.7 and 4-fold realized using the new scheme.
本文描述了一种脉冲序列,用于记录蛋白质中经碳-13(¹³C)选择性标记的甲基基团的单量子(¹³C)甲基弛豫色散曲线。与现有方法相比,该方法具有显著的灵敏度提升,现有方法中初始磁化强度源自¹³C极化。新实验中的灵敏度提升是通过利用氢-1(¹H)自旋的极化以及¹H→¹³C→¹H型磁化转移来实现的。通过涉及三种不同蛋白质系统的应用,已经证明了该方法的实用性,这些蛋白质系统的分子量在8至28 kDa之间,采用了多种不同的选择性标记方法。在所有情况下,来自¹³C→¹H和¹H→¹³C→¹H两类实验的交换参数都吻合良好,使用新方案实现了1.7至4倍的灵敏度提升。