Coy Rachel, Gadêlha Hermes
CoMPLEX, University College London, London WC1E 6BT, UK.
Department of Mathematics, University of York, York YO10 SDD, UK
J R Soc Interface. 2017 May;14(130). doi: 10.1098/rsif.2017.0065.
Cross-linked filament bundles, such as in cilia and flagella, are ubiquitous in biology. They are considered in textbooks as simple filaments with larger stiffness. Recent observations of flagellar counterbend, however, show that induction of curvature in one section of a passive flagellum instigates a compensatory counter-curvature elsewhere, exposing the intricate role of the diminutive cross-linking proteins at large scales. We show that this effect, a material property of the cross-linking mechanics, modifies the bundle dynamics and induces a bimodal - length-dependent material response that departs from the Euler-Bernoulli theory. Hence, the use of simpler theories to analyse experiments can result in paradoxical interpretations. Remarkably, the counterbend dynamics instigates counter-waves in opposition to driven oscillations in distant parts of the bundle, with potential impact on the regulation of flagellar bending waves. These results have a range of physical and biological applications, including the empirical disentanglement of material quantities via counterbend dynamics.
交联丝束,如存在于纤毛和鞭毛中的丝束,在生物学中无处不在。在教科书中,它们被视为具有较大刚度的简单细丝。然而,最近对鞭毛反向弯曲的观察表明,被动鞭毛某一部位的曲率诱导会在其他部位引发补偿性的反向曲率,揭示了微小交联蛋白在大尺度上的复杂作用。我们表明,这种效应作为交联力学的一种材料特性,改变了丝束动力学,并诱导出一种双峰的、长度依赖性的材料响应,这与欧拉 - 伯努利理论不同。因此,使用更简单的理论来分析实验可能会导致矛盾的解释。值得注意的是,反向弯曲动力学在丝束远处引发与驱动振荡相反的反向波,这可能对鞭毛弯曲波的调节产生影响。这些结果具有一系列物理和生物学应用,包括通过反向弯曲动力学对材料量进行实证解缠。