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用有限元法分析“9+2”轴丝的弯曲。

Bending of the "9+2" axoneme analyzed by the finite element method.

机构信息

Er 3 Biogenèse Des Signaux Peptidiques, Université Paris VI, 2, place Jussieu, F-75252 Paris, France.

出版信息

J Theor Biol. 2010 Jun 21;264(4):1089-101. doi: 10.1016/j.jtbi.2010.03.040. Epub 2010 Apr 7.

Abstract

Many data demonstrate that the regulation of the bending polarity of the "9+2" axoneme is supported by the curvature itself, making the internal constraints central in this process, adjusting either the physical characteristics of the machinery or the activity of the enzymes involved in different pathways. Among them, the very integrated Geometric Clutch model founds this regulation on the convenient adjustments of the probability of interaction between the dynein arms and the beta-tubulin monomers of the outer doublet pairs on which they walk. Taking into consideration (i) the deviated bending of the outer doublets pairs (Cibert, C., Heck, J.-V., 2004. Cell Motil. Cytoskeleton 59, 153-168), (ii) the internal tensions of the radial spokes and the tangential links (nexin links, dynein arms), (iii) a theoretical 5 microm long proximal segment of the axoneme and (iv) the short proximal segment of the axoneme, we have reevaluated the adjustments of these intervals using a finite element approach. The movements we have calculated within the axonemal cylinder are consistent with the basic hypothesis that found the Geometric Clutch model, except that the axonemal side where the dynein arms are active increases the intervals between the two neighbor outer doublet pairs. This result allows us to propose a mechanism of bending reversion of the axoneme, involving the concerted ignition of the molecular engines along the two opposite sides of the axoneme delineated by the bending plane.

摘要

许多数据表明,“9+2”轴丝弯曲极性的调节受到曲率本身的支持,使得内部约束成为这一过程的核心,调节的对象包括机械结构的物理特性或参与不同途径的酶的活性。其中,非常整合的几何离合器模型基于以下两个方面来构建这种调节:一是方便调整行走于其上的外二联体对的β-微管蛋白单体与动力蛋白臂之间的相互作用概率;二是考虑到(i)外二联体对的偏斜弯曲(Cibert, C., Heck, J.-V., 2004. Cell Motil. Cytoskeleton 59, 153-168)、(ii)辐条和切线连接(连接蛋白连接、动力蛋白臂)的内部张力、(iii)轴丝近端的理论上 5 μm 长的片段以及(iv)轴丝的短近端片段,我们使用有限元方法重新评估了这些间隔的调整。我们在轴丝筒内计算出的运动与发现几何离合器模型的基本假设一致,但动力蛋白臂活跃的轴丝侧增加了两个相邻外二联体对之间的间隔。这一结果使我们能够提出一种轴丝弯曲反转的机制,涉及沿着弯曲平面两侧的分子发动机的协同点火。

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