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熵力驱动细胞骨架网络的收缩。

Entropic forces drive contraction of cytoskeletal networks.

作者信息

Braun Marcus, Lansky Zdenek, Hilitski Feodor, Dogic Zvonimir, Diez Stefan

机构信息

B CUBE - Center for Molecular Bioengineering, Technische Universität Dresden, Dresden, Germany.

Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.

出版信息

Bioessays. 2016 May;38(5):474-81. doi: 10.1002/bies.201500183. Epub 2016 Mar 21.

Abstract

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.

摘要

细胞骨架是由相互连接的蛋白质细丝组成的网络,为细胞提供三维支架。细胞骨架的重塑对于关键的细胞过程很重要,如细胞运动、分裂或形态发生。传统上认为这种重塑完全由消耗化学能量的过程驱动,如细丝的动态变化或分子马达的作用。在这里,我们回顾两种与化学能量消耗无关的细胞骨架网络重塑机制。在这两种情况下,重叠细丝的定向运动由熵力驱动,熵力源于利用溶液中存在的热能。熵力要么由大分子拥挤剂诱导,要么由局限于细丝重叠区域的可扩散交联剂诱导。这两种机制都增加细丝重叠长度并导致细丝网络收缩。为了全面定量地了解细胞中细胞骨架网络的重塑情况,需要考虑这些产生力的机制以及依赖化学能量的机制。

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