Iovine Joseph C, Alder Nathan N
bioRxiv. 2025 Jun 25:2025.06.23.659572. doi: 10.1101/2025.06.23.659572.
Styrene-maleic acid (SMA) copolymers are powerful tools for the detergent-free solubilization of biological membranes. Yet the influence of specific lipids on SMA activity remains an open question. Here, we examined the effects of the mitochondriaspecific phospholipid cardiolipin on SMA-mediated membrane solubilization and their ability to form SMA-bound nanodiscs. To this end, we prepared a series of model membranes with cardiolipin and other test lipids with comparable surface charge and lateral packing characteristics. Using multiple independent experimental approaches, we found that cardiolipin inhibited SMA solubilization. Our results indicate that this effect was not attributable to headgroup charge effects, but rather to cardiolipininduced increase in lateral packing pressure at the interfacial region. Reduction of this lateral packing pressure using bilayer-active alcohols partially restored SMA solubilization. Our results highlight the importance of lipid geometry and packing in SMA nanodisc formation and could help guide the design of copolymers tailored to specific membranes.
苯乙烯-马来酸(SMA)共聚物是用于无洗涤剂溶解生物膜的有力工具。然而,特定脂质对SMA活性的影响仍是一个悬而未决的问题。在此,我们研究了线粒体特异性磷脂心磷脂对SMA介导的膜溶解作用及其形成SMA结合纳米盘的能力的影响。为此,我们制备了一系列含有心磷脂和其他具有可比表面电荷及侧向堆积特性的测试脂质的模型膜。通过多种独立的实验方法,我们发现心磷脂抑制SMA溶解。我们的结果表明,这种效应并非归因于头基电荷效应,而是由于心磷脂导致界面区域侧向堆积压力增加。使用双层活性醇降低这种侧向堆积压力可部分恢复SMA溶解。我们的结果突出了脂质几何形状和堆积在SMA纳米盘形成中的重要性,并有助于指导针对特定膜定制的共聚物的设计。