Center for Biophysics and Quantitative Biology, University of Illinois at Urbana-Champaign, 314F Roger Adams Laboratory (MC-712), 600 S Mathews Ave, Urbana, IL, 61801, United States; Department of Biochemistry, University of Illinois at Urbana-Champaign, 417 RAL (MC-712), 600 South Mathews Avenue, Urbana, IL, 61801, United States.
Department of Biochemistry, University of Illinois at Urbana-Champaign, 417 RAL (MC-712), 600 South Mathews Avenue, Urbana, IL, 61801, United States.
Chem Phys Lipids. 2019 May;220:28-35. doi: 10.1016/j.chemphyslip.2019.02.008. Epub 2019 Feb 22.
We present a fluorescence-based methodology for monitoring the rotational dynamics of Nanodiscs. Nanodiscs are nano-scale lipid bilayers surrounded by a helical membrane scaffold protein (MSP) that have found considerable use in studying the interactions between membrane proteins and their lipid bilayer environment. Using a long-lifetime Ruthenium label covalently attached to the Nanodiscs, we find that Nanodiscs of increasing diameter, made by varying the number of helical repeats in the MSP, display increasing rotational correlation times. We also model our system using both analytical equations that describe rotating spheroids and numerical calculations performed on atomic models of Nanodiscs. Using these methods, we observe a linear relationship between the experimentally determined rotational correlation times and those calculated from both analytical equations and numerical solutions. This work sets the stage for accurate, label-free quantification of protein-lipid interactions at the membrane surface.
我们提出了一种基于荧光的方法来监测纳米盘的旋转动力学。纳米盘是由螺旋膜支架蛋白(MSP)包围的纳米级脂质双层,在研究膜蛋白与其脂质双层环境之间的相互作用方面有广泛的应用。我们使用共价连接到纳米盘上的长寿命钌标记,发现随着 MSP 中螺旋重复数的增加,直径增大的纳米盘显示出越来越长的旋转相关时间。我们还使用描述旋转球体的解析方程和纳米盘原子模型的数值计算对我们的系统进行建模。使用这些方法,我们观察到实验确定的旋转相关时间与从解析方程和数值解计算得出的旋转相关时间之间存在线性关系。这项工作为在膜表面进行准确、无标记的蛋白质-脂质相互作用定量奠定了基础。