Yip Grover N B, Zuiderweg Erik R P
Department of Chemistry, University of Michigan, 930 N. University Ave., MI 48109-1055, USA.
J Magn Reson. 2005 Oct;176(2):171-8. doi: 10.1016/j.jmr.2005.06.003.
To reliably measure NMR relaxation properties of macromolecules is a prerequisite for precise experiments that identify subtle variations in relaxation rates, as required for the determination of rotational diffusion anisotropy, CSA tensor determination, advanced motional modeling or entropy difference estimations. An underlying problem with current NMR relaxation measurement protocols is maintaining constant sample temperature throughout the execution of the relaxation series especially when rapid data acquisition is required. Here, it is proposed to use a combination of a heating compensation and a proton saturation sequence at the beginning of the NMR relaxation pulse scheme. This simple extension allows reproducible, robust and rapid acquisition of NMR spin relaxation data sets. The method is verified with (15)N spin relaxation measurements for human ubiquitin.
可靠地测量大分子的核磁共振弛豫特性是进行精确实验的前提条件,这些实验需要识别弛豫速率的细微变化,这对于确定旋转扩散各向异性、CSA张量测定、高级运动建模或熵差估计是必需的。当前核磁共振弛豫测量方案的一个潜在问题是,在整个弛豫序列执行过程中保持样品温度恒定,特别是在需要快速数据采集时。在此,建议在核磁共振弛豫脉冲序列开始时结合使用加热补偿和质子饱和序列。这种简单的扩展允许可重复、稳健且快速地采集核磁共振自旋弛豫数据集。该方法通过对人泛素进行¹⁵N自旋弛豫测量得到了验证。