Scheidelaar Stefan, Koorengevel Martijn C, Pardo Juan Dominguez, Meeldijk Johannes D, Breukink Eefjan, Killian J Antoinette
Membrane Biochemistry & Biophysics, Bijvoet Center for Biomolecular Research, Department of Chemistry, Faculty of Science, Utrecht University, Padualaan, Utrecht, The Netherlands.
Membrane Biochemistry & Biophysics, Bijvoet Center for Biomolecular Research, Department of Chemistry, Faculty of Science, Utrecht University, Padualaan, Utrecht, The Netherlands.
Biophys J. 2015 Jan 20;108(2):279-90. doi: 10.1016/j.bpj.2014.11.3464.
A recent discovery in membrane research is the ability of styrene-maleic acid (SMA) copolymers to solubilize membranes in the form of nanodisks allowing extraction and purification of membrane proteins from their native environment in a single detergent-free step. This has important implications for membrane research because it allows isolation as well as characterization of proteins and lipids in a near-native environment. Here, we aimed to unravel the molecular mode of action of SMA copolymers by performing systematic studies using model membranes of varying compositions and employing complementary biophysical approaches. We found that the SMA copolymer is a highly efficient membrane-solubilizing agent and that lipid bilayer properties such as fluidity, thickness, lateral pressure profile, and charge density all play distinct roles in the kinetics of solubilization. More specifically, relatively thin membranes, decreased lateral chain pressure, low charge density at the membrane surface, and increased salt concentration promote the speed and yield of vesicle solubilization. Experiments using a native membrane lipid extract showed that the SMA copolymer does not discriminate between different lipids and thus retains the native lipid composition in the solubilized particles. A model is proposed for the mode of action of SMA copolymers in which membrane solubilization is mainly driven by the hydrophobic effect and is further favored by physical properties of the polymer such as its relatively small cross-sectional area and rigid pendant groups. These results may be helpful for development of novel applications for this new type of solubilizing agent, and for optimization of the SMA technology for solubilization of the wide variety of cell membranes found in nature.
膜研究领域最近的一项发现是,苯乙烯-马来酸(SMA)共聚物能够以纳米盘的形式溶解膜,从而在无需去污剂的单一步骤中从其天然环境中提取和纯化膜蛋白。这对膜研究具有重要意义,因为它能够在近乎天然的环境中分离并表征蛋白质和脂质。在此,我们旨在通过使用不同组成的模型膜并采用互补的生物物理方法进行系统研究,以揭示SMA共聚物的分子作用模式。我们发现SMA共聚物是一种高效的膜溶解剂,脂质双层的性质,如流动性、厚度、横向压力分布和电荷密度,在溶解动力学中都发挥着不同的作用。更具体地说,相对较薄的膜、降低的侧链压力、膜表面的低电荷密度以及增加的盐浓度会促进囊泡溶解的速度和产率。使用天然膜脂质提取物进行的实验表明,SMA共聚物不会区分不同的脂质,因此在溶解颗粒中保留了天然脂质组成。我们提出了一个SMA共聚物作用模式的模型,其中膜溶解主要由疏水效应驱动,并进一步受到聚合物物理性质的青睐,如相对较小的横截面积和刚性侧基。这些结果可能有助于开发这种新型溶解剂的新应用,并优化SMA技术以溶解自然界中发现的各种细胞膜。