Center for Biophysics and Computational Biology, University of Illinois, Urbana, IL 61801, USA.
Biochemistry. 2010 Nov 2;49(43):9190-8. doi: 10.1021/bi1013722.
Nanodiscs are examples of discoidal nanoscale lipid-protein particles that have been extremely useful for the biochemical and biophysical characterization of membrane proteins. They are discoidal lipid bilayer fragments encircled and stabilized by two amphipathic helical proteins named membrane scaffolding protein (MSP), ~10 nm in size. Nanodiscs are homogeneous, easily prepared with reproducible success, amenable to preparations with a variety of lipids, and stable over a range of temperatures. Here we present solid-state nuclear magnetic resonance (SSNMR) studies on lyophilized, rehydrated POPC Nanodiscs prepared with uniformly (13)C-, (15)N-labeled MSP1D1 (Δ1-11 truncated MSP). Under these conditions, by SSNMR we directly determine the gel-to-liquid crystal lipid phase transition to be at 3 ± 2 °C. Above this phase transition, the lipid (1)H signals have slow transverse relaxation, enabling filtering experiments as previously demonstrated for lipid vesicles. We incorporate this approach into two- and three-dimensional heteronuclear SSNMR experiments to examine the MSP1D1 residues interfacing with the lipid bilayer. These (1)H-(13)C and (1)H-(13)C-(13)C correlation spectra are used to identify and quantify the number of lipid-correlated and solvent-exposed residues by amino acid type, which furthermore is compared with molecular dynamics studies of MSP1D1 in Nanodiscs. This study demonstrates the utility of SSNMR experiments with Nanodiscs for examining lipid-protein interfaces and has important applications for future structural studies of membrane proteins in physiologically relevant formulations.
纳米盘是碟状纳米级脂质-蛋白颗粒的示例,对于膜蛋白的生化和生物物理特性分析非常有用。它们是由两个两亲性螺旋蛋白(称为膜支架蛋白,MSP)环绕和稳定的碟状脂质双层片段,大小约为 10nm。纳米盘是均相的,易于制备且重复性好,可与多种脂质一起制备,并且在一定温度范围内稳定。在这里,我们介绍了使用均一(13)C-,(15)N-标记的 MSP1D1(Δ1-11 截断 MSP)制备的冻干、复水的 POPC 纳米盘的固态核磁共振(SSNMR)研究。在这些条件下,通过 SSNMR 我们直接确定凝胶到液晶脂质相转变温度为 3±2°C。在这个相变温度以上,脂质(1)H 信号的横向弛豫缓慢,能够像以前对脂质体所证明的那样进行过滤实验。我们将这种方法应用于二维和三维异核 SSNMR 实验中,以研究与脂质双层相互作用的 MSP1D1 残基。这些(1)H-(13)C 和(1)H-(13)C-(13)C 相关谱用于通过氨基酸类型来识别和量化与脂质相关和溶剂暴露的残基的数量,并且与 MSP1D1 在纳米盘中的分子动力学研究进行了比较。该研究证明了使用纳米盘进行 SSNMR 实验研究脂质-蛋白界面的有效性,并且对于在生理相关配方中研究膜蛋白的未来结构具有重要意义。