Lateral lipid packing governs bilayer solubilization by styrene-maleic acid copolymers: a case study with cardiolipin-containing membranes.

IF 2.5 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Joseph C Iovine, Benjamin T Garrett, Nathan N Alder
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引用次数: 0

Abstract

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 mitochondria-specific phospholipid cardiolipin on SMA-mediated membrane solubilization and its 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 related to cardiolipin-induced 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.

侧脂质填料支配着苯乙烯-马来酸共聚物的双层增溶:含心磷脂膜的案例研究。
苯乙烯-马来酸(SMA)共聚物是生物膜无洗涤剂增溶的有力工具。然而,特定脂类对SMA活性的影响仍然是一个悬而未决的问题。在这里,我们研究了线粒体特异性磷脂心磷脂对sma介导的膜增溶及其形成sma结合纳米盘的能力的影响。为此,我们制备了一系列模型膜,其中含有心磷脂和其他具有类似表面电荷和横向包装特性的测试脂质。通过多个独立的实验方法,我们发现心磷脂抑制SMA的增溶。我们的研究结果表明,这种影响不是归因于头群电荷效应,而是与心磷脂诱导的界面区域侧堆积压力的增加有关。使用双层活性醇降低侧封压力,部分恢复了SMA的增溶作用。我们的研究结果强调了脂质几何形状和填充在SMA纳米盘形成中的重要性,并有助于指导针对特定膜定制共聚物的设计。
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来源期刊
Biochimica et biophysica acta. Biomembranes
Biochimica et biophysica acta. Biomembranes 生物-生化与分子生物学
CiteScore
8.20
自引率
5.90%
发文量
175
审稿时长
2.3 months
期刊介绍: BBA Biomembranes has its main focus on membrane structure, function and biomolecular organization, membrane proteins, receptors, channels and anchors, fluidity and composition, model membranes and liposomes, membrane surface studies and ligand interactions, transport studies, and membrane dynamics.
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