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动态组合:凝聚相-脂质膜相互作用在调节膜转化和凝聚物大小方面的作用

Dynamic Duos: Coacervate-Lipid Membrane Interactions in Regulating Membrane Transformation and Condensate Size.

作者信息

Nair Karthika S, Radhakrishnan Sreelakshmi, Bajaj Harsha

机构信息

Microbial Processes and Technology Division, CSIR-National Institute for Interdisciplinary Science and Technology (NIIST), Trivandrum, Kerala, 695019, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad-201002, India.

出版信息

Small. 2025 May;21(20):e2501470. doi: 10.1002/smll.202501470. Epub 2025 Mar 30.

DOI:10.1002/smll.202501470
PMID:40159770
Abstract

Biomolecular condensates interfacing with lipid membranes is crucial for several key cellular functions. However, the role of lipid membranes in regulating condensates in cells remains obscure. Here, in-depth interactions between condensates and lipid membranes are probed and unraveled by employing cell-mimetic systems like Giant unilamellar vesicles (GUVs). An unprecedented influence of the coacervate size and their electrostatic interaction with lipid membranes is revealed on the membrane properties and deformation. Importantly, these findings demonstrate that the large relative size of coacervates and minimal electrostatic interaction strength with membranes allow for budding transitions at the interface. Membranes act as nucleation site for coacervates when the charge-charge interaction is high, giving a wrinkled vesicle surface appearance. Molecular diffusion property of lipids, quantified using Fluorescence recovery after photobleaching (FRAP), is modulated at the coacervate-membrane interaction site restricting the coarsening of coacervates. Notably, these results reveal coacervate droplets are intertwined in between membrane folds and invaginations discerned using Transmission electron microscopy (TEM) and high-resolution imaging, which further controls the dimension of droplets resembling size distributions observed in cells. Finally, these findings provide mechanistic insights of lipid bilayers controlling condensate sizes that play a prominent role in comprehending nucleation and localization of cellular condensates.

摘要

生物分子凝聚物与脂质膜的相互作用对几个关键的细胞功能至关重要。然而,脂质膜在调节细胞内凝聚物方面的作用仍不清楚。在这里,通过使用巨型单层囊泡(GUVs)等细胞模拟系统,深入探究并揭示了凝聚物与脂质膜之间的相互作用。研究发现凝聚物的大小及其与脂质膜的静电相互作用对膜的性质和变形有着前所未有的影响。重要的是,这些发现表明,凝聚物的相对尺寸较大且与膜的静电相互作用强度最小,使得在界面处能够发生出芽转变。当电荷 - 电荷相互作用较高时,膜充当凝聚物的成核位点,导致囊泡表面出现褶皱。使用光漂白后荧光恢复(FRAP)定量的脂质分子扩散特性在凝聚物 - 膜相互作用位点受到调节,从而限制了凝聚物的粗化。值得注意的是,这些结果表明凝聚物液滴交织在膜褶皱和内陷之间,这可以通过透射电子显微镜(TEM)和高分辨率成像观察到,这进一步控制了液滴的尺寸,类似于在细胞中观察到的大小分布。最后,这些发现为脂质双层控制凝聚物大小提供了机制性见解,这在理解细胞凝聚物的成核和定位方面起着重要作用。

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