Fürthauer Sebastian, Lemma Bezia, Foster Peter J, Ems-McClung Stephanie C, Yu Che-Hang, Walczak Claire E, Dogic Zvonimir, Needleman Daniel J, Shelley Michael J
Center for Computational Biology, Flatiron Institute, New York, NY, USA.
Department of Physics, Harvard University, Cambridge, MA, USA.
Nat Phys. 2019 Dec;15(12):1295-1300. doi: 10.1038/s41567-019-0642-1. Epub 2019 Sep 2.
Cytoskeletal networks are foundational examples of active matter and central to self-organized structures in the cell. In vivo, these networks are active and densely crosslinked. Relating their large-scale dynamics to the properties of their constituents remains an unsolved problem. Here, we study an in vitro active gel made from aligned microtubules and XCTK2 kinesin motors. Using photobleaching, we demonstrate that the gel's aligned microtubules, driven by motors, continually slide past each other at a speed independent of the local microtubule polarity and motor concentration. This phenomenon is also observed, and remains unexplained, in spindles. We derive a general framework for coarse graining microtubule gels crosslinked by molecular motors from microscopic considerations. Using microtubule-microtubule coupling through a force-velocity relationship for kinesin, this theory naturally explains the experimental results: motors generate an active strain rate in regions of changing polarity, which allows microtubules of opposite polarities to slide past each other without stressing the material.
细胞骨架网络是活性物质的基础示例,也是细胞中自组织结构的核心。在体内,这些网络是活跃且高度交联的。将它们的大规模动力学与其组成成分的特性联系起来仍然是一个未解决的问题。在这里,我们研究了一种由排列的微管和XCTK2驱动蛋白马达制成的体外活性凝胶。通过光漂白,我们证明,由马达驱动的凝胶排列微管以独立于局部微管极性和马达浓度的速度持续相互滑过。这种现象在纺锤体中也有观察到,但仍无法解释。我们从微观角度推导出了一个用于粗粒化由分子马达交联的微管凝胶的通用框架。利用驱动蛋白通过力 - 速度关系实现的微管 - 微管耦合,该理论自然地解释了实验结果:马达在极性变化区域产生活性应变率,这使得相反极性的微管能够相互滑过而不会使材料受力。