Marsan M P, Muller I, Ramos C, Rodriguez F, Dufourc E J, Czaplicki J, Milon A
Institut de Pharmacologie et de Biologie Structurale, CNRS, 205 rte de Narbonne, 31077 Toulouse, France.
Biophys J. 1999 Jan;76(1 Pt 1):351-9. doi: 10.1016/S0006-3495(99)77202-4.
Proton decoupled deuterium NMR spectra of oriented bilayers made of DMPC and 30 mol % deuterated cholesterol acquired at 76.8 MHz (30 degreesC) have provided a set of very accurate quadrupolar splitting for eight C-D bonds of cholesterol. Due to the new precision of the experimental data, the original analysis by. Biochemistry. 23:6062-6071) had to be reconsidered. We performed a systematic study of the influence on the precision and uniqueness of the data-fitting procedure of: (i) the coordinates derived from x-ray, neutron scattering, or force field-minimized structures, (ii) internal mobility, (iii) the axial symmetry hypothesis, and (iv) the knowledge of some quadrupolar splitting assignments. Good agreement between experiment and theory could be obtained only with the neutron scattering structure, for which both axial symmetry hypothesis and full order parameter matrix analysis gave satisfactory results. Finally, this work revealed an average orientation of cholesterol slightly different from those previously published and, most importantly, a molecular order parameter equal to 0.95 +/- 0.01, instead of 0.79 +/- 0.03 previously found for the same system at 30 degreesC. Temperature dependence in the 20-50 degreesC range shows a constant average orientation and a monotonous decrease of cholesterol Smol, with a slope of -0.0016 K-1. A molecular order parameter of 0.89 +/- 0.01 at 30 degreesC was determined for a DMPC/16 mol % of cholesterol.
在76.8兆赫(30℃)下获得的由二肉豆蔻酰磷脂酰胆碱(DMPC)和30摩尔%氘代胆固醇构成的取向双层膜的质子去耦氘核磁共振谱,为胆固醇的八个C-D键提供了一组非常精确的四极分裂数据。由于实验数据的新精度,《生物化学》(23:6062 - 6071)中的原始分析必须重新考虑。我们对以下因素对数据拟合程序的精度和唯一性的影响进行了系统研究:(i)从X射线、中子散射或力场最小化结构导出的坐标;(ii)内部流动性;(iii)轴对称假设;(iv)一些四极分裂归属的知识。只有使用中子散射结构才能使实验与理论取得良好的一致性,对于该结构,轴对称假设和全序参数矩阵分析都给出了令人满意的结果。最后,这项工作揭示了胆固醇的平均取向与先前发表的略有不同,最重要的是,分子序参数为0.95±0.01,而不是先前在30℃下对同一系统所发现的0.79±0.03。在20 - 50℃范围内的温度依赖性显示胆固醇的平均取向恒定,而其序参数单调下降,斜率为 - 0.0016 K⁻¹。对于DMPC/16摩尔%胆固醇体系,在30℃下测定的分子序参数为0.89±0.01。