论文标题

捆绑肌动蛋白网络耗尽驱动的形态控制

Depletion-Driven Morphological Control of Bundled Actin Networks

论文作者

Clarke, James, Cavanna, Francis, Crowell, Anne D., Melcher, Lauren, Houser, Justin R., Graham, Kristin, Green, Allison, Stachowiak, Jeanne C., Truskett, Thomas M., Milliron, Delia J., Rosales, Adrianne M., Das, Moumita, Alvarado, José

论文摘要

肌动蛋白细胞骨架是一个半融合的生物聚合物网络,其形态受到多种生化和物理因素的控制。已知肌动蛋白通过在足够浓度的情况下添加聚乙烯乙二醇(PEG)分子,从而经历从单丝状状态到捆绑状态的相过渡。尽管这些生物聚合物经历的耗尽相互作用是众所周知的,但改变消耗剂的分子量的效果知之甚少。在这里,我们通过改变PEG聚合物的分子量,同时保持这些PEG聚合物的浓度恒定,从实验中确定肌动蛋白溶液中从细丝网络到束束网络的相变。我们检查以微观和宏观特性方面跨越相变的状态。我们发现,在整个临界行的细丝之间的细丝之间的网格大小,束直径,持久性长度和束内间距不会显示出显着差异,而放松时间,存储模量和两个州之间的捆绑变化程度确实显示出显着差异。我们的结果表明,通过控制消耗大小来调整肌动蛋白网络形态和力学的能力,该属性可以利用,以开发具有可切换刚度的基于肌动蛋白的材料。

The actin cytoskeleton is a semiflexible biopolymer network whose morphology is controlled by a wide range of biochemical and physical factors. Actin is known to undergo a phase transition from a single-filament state to a bundled state by the addition of polyethylene glycol (PEG) molecules in sufficient concentration. While the depletion interaction experienced by these biopolymers is well-known, the effect of changing the molecular weight of the depletant is less well understood. Here, we experimentally identify a phase transition in solutions of actin from networks of filaments to networks of bundles by varying the molecular weight of PEG polymers, while holding the concentration of these PEG polymers constant. We examine the states straddling the phase transition in terms of micro and macroscale properties. We find that the mesh size, bundle diameter, persistence length, and intra-bundle spacing between filaments across the line of criticality do not show significant differences, while the relaxation time, storage modulus, and degree of bundling change between the two states do show significant differences. Our results demonstrate the ability to tune actin network morphology and mechanics by controlling depletant size, a property which could be exploited to develop actin-based materials with switchable rigidity.

扫码加入交流群

加入微信交流群

微信交流群二维码

扫码加入学术交流群,获取更多资源