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预湿使膜和蛋白质相变耦合,从而极大地增强了模型和细胞中的共存现象。

Prewetting couples membrane and protein phase transitions to greatly enhance coexistence in models and cells.

作者信息

Bagheri Yousef, Rouches Mason, Machta Benjamin, Veatch Sarah L

机构信息

Program in Biophysics, University of Michigan, Ann Arbor, MI USA.

Department of Molecular Biophysics & Biochemistry, Yale University, New Haven CT USA.

出版信息

bioRxiv. 2024 Aug 27:2024.08.26.609758. doi: 10.1101/2024.08.26.609758.

Abstract

Both membranes and biopolymers can individually separate into coexisting liquid phases. Here we explore biopolymer prewetting at membranes, a phase transition that emerges when these two thermodynamic systems are coupled. In reconstitution, we couple short poly-L-Lysine and poly-L-Glutamic Acid polyelectrolytes to membranes of saturated lipids, unsaturated lipids, and cholesterol, and detect coexisting prewet and dry surface phases well outside of the region of coexistence for each individual system. Notability, polyelectrolyte prewetting is highly sensitive to membrane lipid composition, occurring at 10 fold lower polymer concentration in a membrane close to its phase transition compared to one without a phase transition. In cells, protein prewetting is achieved using an optogenetic tool that enables titration of condensing proteins and tethering to the plasma membrane inner leaflet. Here we show that protein prewetting occurs for conditions well outside those where proteins condense in the cytoplasm, and that the stability of prewet domains is sensitive to perturbations of plasma membrane composition and structure. Our work presents an example of how thermodynamic phase transitions can impact cellular structure outside their individual coexistence regions, suggesting new possible roles for phase-separation-prone systems in cell biology.

摘要

膜和生物聚合物都能各自分离成共存的液相。在此,我们探索膜上的生物聚合物预湿润现象,这是当这两个热力学系统耦合时出现的一种相变。在重构过程中,我们将短聚-L-赖氨酸和聚-L-谷氨酸聚电解质与饱和脂质、不饱和脂质和胆固醇的膜耦合,并检测到在每个单独系统共存区域之外存在的预湿润和干燥表面相。值得注意的是,聚电解质预湿润对膜脂质组成高度敏感,与无相变的膜相比,在接近其相变的膜中,聚合物浓度低10倍时就会发生预湿润。在细胞中,使用光遗传学工具实现蛋白质预湿润,该工具能够滴定凝聚蛋白并将其拴系到质膜内小叶上。在此我们表明,蛋白质预湿润发生在蛋白质在细胞质中凝聚的条件之外,并且预湿润域的稳定性对质膜组成和结构的扰动敏感。我们的工作展示了热力学相变如何在其各自的共存区域之外影响细胞结构的一个例子,这暗示了易于发生相分离的系统在细胞生物学中的新潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fce/11383005/4124e131d63c/nihpp-2024.08.26.609758v1-f0001.jpg

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