Brokaw C J
Symp Soc Exp Biol. 1982;35:313-38.
A computer program for simulating the movement of model flagella containing a four-state cross-bridge cycle provides a powerful tool for examining hypotheses about the control mechanisms involved in producing particular patterns of propagated bending. As learned previously with simpler models, a simple control of cross-bridge activity by curvature is sufficient to generate spontaneous oscillation and bend propagation, but fails to reproduce many important features of the behaviour of real flagella. The process of bend initiation can be isolated by studying the movement of demembranated sea urchin sperm flagella broken to lengths of 3-4 microns, and by studying the movement of the distal end of a flagellum when most of the length of the flagellum becomes stuck to a surface. In order to simulate the movement seen in these situations, at least one major modification of the control of cross-bridge activity appears to be necessary. When a new bend is forming, the active sliding of cross-bridges causing the bend to form can be turned off when the curvature of the bend reaches a critical value, as in the earlier models. However, the active sliding of cross-bridges in the opposite direction, which will cause propagation of the bend, does not appear to be turned on at the same time. The mechanisms which trigger this delayed activation of cross-bridges almost simultaneously throughout the length of a newly formed bend have not yet been identified. They are presumably the same as those involved in activating sliding throughout most of the length of a flagellum at the beginning of its effective stroke.
一个用于模拟包含四态横桥循环的模型鞭毛运动的计算机程序,为检验有关产生特定传播弯曲模式的控制机制的假设提供了一个强大的工具。正如之前用更简单的模型所了解到的,通过曲率对横桥活动进行简单控制足以产生自发振荡和弯曲传播,但无法再现真实鞭毛行为的许多重要特征。弯曲起始过程可以通过研究断裂成3 - 4微米长度的去膜海胆精子鞭毛的运动,以及通过研究当鞭毛大部分长度粘在表面时鞭毛远端的运动来分离。为了模拟在这些情况下看到的运动,横桥活动控制至少需要一项重大修改。当新的弯曲形成时,如早期模型那样,当弯曲的曲率达到临界值时,可关闭导致弯曲形成的横桥的主动滑动。然而,会导致弯曲传播的相反方向的横桥主动滑动似乎不会同时开启。在新形成的弯曲的整个长度上几乎同时触发这种横桥延迟激活的机制尚未确定。它们大概与在有效冲程开始时在鞭毛大部分长度上激活滑动所涉及的机制相同。