James Franck Institute, The University of Chicago, Chicago, IL 60637, USA.
Soft Matter. 2020 Feb 26;16(8):2135-2140. doi: 10.1039/c9sm01904a.
Within cells, crosslinking proteins organize cytoskeletal filaments both temporally and spatially to create dynamic and structurally diverse networks. Molecular motors move on these networks for both force generation and transport processes. How the transport statistics depend on the network architecture remains poorly characterized. Using cross-linking proteins (α-actinin, fimbrin, fascin, or filamin) and purified actin, we create cytoskeletal networks with diverse microscopic architectures. We track the motion of myosin II motor proteins moving on these networks and calculate transport statistics. We observe that motor dynamics change predictably based on the bundling of filaments within the underlying networks and discuss implications for network function.
在细胞内,交联蛋白在时间和空间上组织细胞骨架丝,以创建动态和结构多样的网络。分子马达在这些网络上移动,以进行力生成和运输过程。运输统计数据如何依赖于网络架构仍然知之甚少。我们使用交联蛋白(α-肌动蛋白、 fimbrin、 fascin 或 filamin)和纯化的肌动蛋白,创建具有不同微观结构的细胞骨架网络。我们跟踪在这些网络上移动的肌球蛋白 II 运动蛋白的运动,并计算运输统计数据。我们观察到,基于基础网络中纤维的束状结构,马达动力学发生可预测的变化,并讨论了对网络功能的影响。