Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Department of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Methods. 2018 Apr 1;138-139:47-53. doi: 10.1016/j.ymeth.2018.01.008. Epub 2018 Feb 21.
Cholesterol (Chol) is vital for cell function as it is essential to a myriad of biochemical and biophysical processes. The atomistic details of Chol's interactions with phospholipids and proteins is therefore of fundamental interest, and NMR offers unique opportunities to interrogate these properties at high resolution. Towards this end, here we describe approaches for examining the structure and dynamics of Chol in lipid bilayers using high levels of C enrichment in combination with magic-angle spinning (MAS) methods. We quantify the incorporation levels and demonstrate high sensitivity and resolution in 2D C-C and H-C spectra, enabling de novo assignments and site-resolved order parameter measurements obtained in a fraction of the time required for experiments with natural abundance sterols. We envision many potential future applications of these methods to study sterol interactions with drugs, lipids and proteins.
胆固醇(Chol)对于细胞功能至关重要,因为它是无数生化和生物物理过程所必需的。因此,Chol 与磷脂和蛋白质相互作用的原子细节具有根本的重要性,而 NMR 提供了独特的机会,可以在高分辨率下研究这些性质。为此,本文描述了使用高水平的 C 丰度结合魔角旋转(MAS)方法研究脂质双层中 Chol 结构和动力学的方法。我们定量了掺入水平,并在 2D C-C 和 H-C 谱中展示了高灵敏度和分辨率,使从头分配和位分辨有序参数测量在所需时间的一小部分内完成,而使用天然丰度固醇进行实验则需要大量时间。我们设想这些方法在研究固醇与药物、脂质和蛋白质相互作用方面有许多潜在的未来应用。