Allard P, Jarvet J, Ehrenberg A, Gräslund A
Department of Biophysics, Arrhenius Laboratories, Stockholm University, Sweden.
J Biomol NMR. 1995 Feb;5(2):133-46. doi: 10.1007/BF00208804.
The peptide hormone motilin was synthesised with a 13C-enriched alpha-carbon in the leucine at position 10. In aqueous solution, six different relaxation rates were measured for the 13C alpha-H alpha fragment as a function of temperature and with and without the addition of 30% (v/v) of the cosolvent d2-1,1,1,3,3,3-hexafluoro-2-propanol (HFP). The relaxation rates were analysed employing the spectral density mapping technique introduced by Peng and Wagner [(1992) J. Magn. Reson., 98, 308-332] and using the model-free approach by Lipari and Szabo [(1982) J. Am. Chem. Soc., 104, 4546-4570]. The fit to various models of dynamics was also considered. Different procedures to evaluate the overall rotational correlation time were compared. A single exponential time correlation function was found to give a good fit to the measured spectral densities only for motilin in 30% (v/v) HFP at low temperatures, whereas at high temperatures in this solvent, and in D2O at all temperatures, none of the considered models gave an acceptable fit. A new empirical spectral density function was tested and found to accurately fit the experimental spectral density mapping points. The application of spectral density mapping based on NMR relaxation data for a specific 13C-1H vector is shown to be a highly useful method to study biomolecular dynamics. Advantages are high sensitivity, high precision and uniform sampling of the spectral density function over the frequency range.
肽激素胃动素在第10位亮氨酸的α-碳上用富含13C的物质合成。在水溶液中,测量了13Cα-Hα片段在有和没有添加30%(v/v)的助溶剂d2-1,1,1,3,3,3-六氟-2-丙醇(HFP)的情况下,作为温度函数的六种不同的弛豫率。采用Peng和Wagner[(1992)J.Magn.Reson.,98,308 - 332]引入的谱密度映射技术并使用Lipari和Szabo[(1982)J.Am.Chem.Soc.,104,4546 - 4570]的无模型方法对弛豫率进行了分析。还考虑了对各种动力学模型的拟合。比较了评估整体旋转相关时间的不同程序。发现仅在低温下30%(v/v)HFP中的胃动素,单指数时间相关函数能很好地拟合测量的谱密度,而在该溶剂的高温下以及在所有温度下的D2O中,所考虑的模型均未给出可接受的拟合。测试了一种新的经验谱密度函数,发现它能准确拟合实验谱密度映射点。基于特定13C-1H向量的NMR弛豫数据的谱密度映射应用被证明是研究生物分子动力学的一种非常有用的方法。优点是灵敏度高、精度高以及在频率范围内对谱密度函数进行均匀采样。