Umegawa Yuichi, Yamaguchi Toshiyuki, Murata Michio, Matsuoka Shigeru
JST ERATO, Lipid Active Structure Project, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka Prefecture, 560-0043, Japan.
Department of Chemistry, Graduate School of Science, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka Prefecture, 560-0043, Japan.
Magn Reson Chem. 2015 Jul;53(7):514-9. doi: 10.1002/mrc.4247. Epub 2015 May 27.
Structural diversity and molecular flexibility of phospholipids are essential for biological membranes to play key roles in numerous cellular processes. Uncovering the behavior of individual lipids in membrane dynamics is crucial for understanding the molecular mechanisms underlying biological functions of cell membranes. In this paper, we introduce a simple method to investigate dynamics of lipid molecules in multi-component systems by measuring the (31) P chemical shift anisotropy (CSA) under magic angle spinning (MAS) conditions. For achieving both signal separation and CSA determination, we utilized a centerband-only analysis of rotor-unsynchronized spin echo (COARSE). This analysis is based on the curve fitting of periodic modulation of centerband intensity along the interpulse delay time in rotor-unsynchronized spin-echo experiments. The utility of COARSE was examined by using phospholipid vesicles, a three-component lipid raft model system, and archaeal purple membranes. We found that the apparent advantages of this method are high resolution and high sensitivity given by the moderate MAS speed and the one-dimensional acquisition with short spin-echo delays. COARSE provides an alternative method for CSA measurement that is effective in the investigation of lipid polymorphologies.
磷脂的结构多样性和分子灵活性对于生物膜在众多细胞过程中发挥关键作用至关重要。揭示单个脂质在膜动力学中的行为对于理解细胞膜生物学功能的分子机制至关重要。在本文中,我们介绍了一种简单的方法,通过在魔角旋转(MAS)条件下测量(31)P化学位移各向异性(CSA)来研究多组分系统中脂质分子的动力学。为了实现信号分离和CSA测定,我们采用了仅对转子非同步自旋回波进行中心带分析(COARSE)。该分析基于转子非同步自旋回波实验中沿脉冲间隔时间的中心带强度周期性调制的曲线拟合。通过使用磷脂囊泡、三组分脂筏模型系统和古菌紫膜来检验COARSE的实用性。我们发现该方法的明显优势在于适度的MAS速度和短自旋回波延迟的一维采集所带来的高分辨率和高灵敏度。COARSE为CSA测量提供了一种替代方法,在研究脂质多晶型方面很有效。