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Entropic forces drive contraction of cytoskeletal networks

机译:熵力驱动细胞骨架网络的收缩

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摘要

The cytoskeleton is a network of interconnected protein filaments, which provide a three-dimensional scaffold for cells. Remodeling of the cytoskeleton is important for key cellular processes, such as cell motility, division, or morphogenesis. This remodeling is traditionally considered to be driven exclusively by processes consuming chemical energy, such as the dynamics of the filaments or the action of molecular motors. Here, we review two mechanisms of cytoskeletal network remodeling that are independent of the consumption of chemical energy. In both cases directed motion of overlapping filaments is driven by entropic forces, which arise from harnessing thermal energy present in solution. Entropic forces are induced either by macromolecular crowding agents or by diffusible crosslinkers confined to the regions where filaments overlap. Both mechanisms increase filament overlap length and lead to the contraction of filament networks. These force-generating mechanisms, together with the chemical energy-dependent mechanisms, need to be considered for the comprehensive quantitative picture of the remodeling of cytoskeletal networks in cells.
机译:细胞骨架是相互连接的蛋白丝的网络,这些蛋白丝为细胞提供了三维支架。细胞骨架的重塑对于关键的细胞过程(例如细胞运动,分裂或形态发生)很重要。传统上,这种重塑仅由消耗化学能的过程来驱动,例如长丝的动力学或分子马达的作用。在此,我们回顾了细胞骨架网络重塑的两种机制,这些机制与化学能的消耗无关。在这两种情况下,重叠长丝的定向运动都是由熵力驱动的,熵力是利用溶液中存在的热能而产生的。熵力是由大分子拥挤剂引起的,或者由限制在长丝重叠区域的可扩散交联剂引起的。两种机理都增加了细丝的重叠长度,并导致细丝网络的收缩。这些力产生机制,以及化学能依赖性机制,需要考虑用于细胞中细胞骨架网络重塑的全面定量图像。

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