Soubias O, Piotto M, Saurel O, Assemat O, Réat V, Milon A
Institut de Pharmacologie et de Biologie Structurale, CNRS and UPS, UMR 5089 205 rte de Narbonne, 31077 Toulouse, Cedex 4, France.
J Magn Reson. 2003 Dec;165(2):303-8. doi: 10.1016/j.jmr.2003.08.001.
The quality and signal to noise ratio of a J-based HETCOR performed on a standard MAS probe have been compared with a gradient enhanced HSQC performed on a HR-MAS probe at 500 MHz. The sample selected was cholesterol, inserted at 30 mol% in acyl chain deuterated phospholipids (DMPC-d54), at a temperature where the bilayer is in a liquid crystalline phase (310 K). It is representative of any rigid molecule undergoing fast axial diffusion in a bilayer as the main movement. After optimization of the spinning rate and carbon decoupling conditions, it is shown that the ge-HSQC/MAS approach is far superior to the more conventional J-HETCOR/MAS in terms of signal to noise ratio, and that it allows the detection of all the natural abundance cross peaks of cholesterol in a membrane environment. Clear differences between the 1H and 13C chemical shifts of cholesterol in a membrane and in chloroform solution were thus revealed.
在标准MAS探头下进行的基于J的HETCOR实验的质量和信噪比,已与在500 MHz的HR-MAS探头下进行的梯度增强HSQC实验进行了比较。所选样品为胆固醇,以30 mol%的比例插入酰基链氘代磷脂(DMPC-d54)中,温度设定为双层处于液晶相的温度(310 K)。它代表了任何在双层中以快速轴向扩散为主要运动形式的刚性分子。在优化了自旋速率和碳去耦条件后,结果表明,就信噪比而言,ge-HSQC/MAS方法远比传统的J-HETCOR/MAS方法优越,并且它能够检测膜环境中胆固醇的所有天然丰度交叉峰。由此揭示了胆固醇在膜中和氯仿溶液中的1H和13C化学位移之间的明显差异。