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脂膜形貌是液-液相分离蛋白凝聚体空间分布的调控者。

Lipid Membrane Topographies Are Regulators for the Spatial Distribution of Liquid Protein Condensates.

机构信息

Biophysics, Max Planck Institute for the Science of Light, 91058 Erlangen, Germany.

出版信息

Nano Lett. 2024 Apr 17;24(15):4330-4335. doi: 10.1021/acs.nanolett.3c04169. Epub 2024 Apr 5.

Abstract

Liquid protein condensates play important roles in orchestrating subcellular organization and as biochemical reaction hubs. Recent studies have linked lipid membranes to proteins capable of forming liquid condensates, and shown that biophysical parameters, like protein enrichment and restricted diffusion at membranes, regulate condensate formation and size. However, the impact of membrane topography on liquid condensates remains poorly understood. Here, we devised a cell-free system to reconstitute liquid condensates on lipid membranes with microstructured topographies and demonstrated that lipid membrane topography is a significant biophysical regulator. Using membrane surfaces designed with microwells, we observed ordered condensate patterns. Furthermore, we demonstrate that membrane topographies influence the shape of liquid condensates. Finally, we show that capillary forces, mediated by membrane topographies, lead to the directed fusion of liquid condensates. Our results demonstrate that membrane topography is a potent biophysical regulator for the localization and shape of mesoscale liquid protein condensates.

摘要

液体蛋白凝聚物在协调细胞内组织和作为生化反应中心方面发挥着重要作用。最近的研究将脂质膜与能够形成液体凝聚物的蛋白质联系起来,并表明生物物理参数,如蛋白质富集和膜扩散受限,调节凝聚物的形成和大小。然而,膜拓扑结构对液体凝聚物的影响仍知之甚少。在这里,我们设计了一种无细胞系统,在具有微结构拓扑的脂质膜上重新构建液体凝聚物,并证明脂质膜拓扑结构是一个重要的生物物理调节剂。使用设计有微井的膜表面,我们观察到有序的凝聚物图案。此外,我们证明了膜拓扑结构会影响液体凝聚物的形状。最后,我们表明,由膜拓扑结构介导的毛细力导致液体凝聚物的定向融合。我们的结果表明,膜拓扑结构是定位和形状的中尺度液体蛋白凝聚物的有力生物物理调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e28b/11036382/86775796e078/nl3c04169_0001.jpg

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