Jarosch R, Foissner I
Eur J Cell Biol. 1982 Feb;26(2):295-302.
Simple model experiments show that the cyclic motion of myosin cross-bridges in muscle which is assumed to be active ("sliding model" by "power-stroke" or "rowing-stroke" of the crossbridges) can be interpreted equally well as a passive process during which the myosin heads simply lock mechanically into the grooves of the thin filaments. In order to explain the sliding process a filament or microtubule rotation is assumed to be combined with the winding and unwinding of associated helical protein filaments ("MAPs", "dynein"). As shown in further model experiments the direction of helix winding or unwinding along a rod (microtubule) determines the direction of rod displacement ("parallel" or "antiparallel sliding"). The "sidearms" and "bridges" visible in the electron microscope along the cytoskeletal elements might correspond to the winding or unwinding filaments. On the basis of this conception simple models for the behavior of spindle microtubules and the anaphase movement of chromosomes are presented. The latter is assumed to occur via the unwinding of helical filaments accompanying the kinetochore microtubules, which causes their simultaneous depolymerization.
简单的模型实验表明,肌肉中肌球蛋白横桥的循环运动(假定为活跃的,即通过横桥的“动力冲程”或“划桨冲程”实现的“滑动模型”)同样可以被解释为一个被动过程,在此过程中,肌球蛋白头部只是机械地锁定在细肌丝的凹槽中。为了解释滑动过程,假定细丝或微管的旋转与相关螺旋状蛋白质细丝(“微管相关蛋白”、“动力蛋白”)的缠绕和解缠绕相结合。如进一步的模型实验所示,沿着杆(微管)的螺旋缠绕或解缠绕方向决定了杆的位移方向(“平行”或“反平行滑动”)。在电子显微镜下沿着细胞骨架元件可见的“侧臂”和“桥”可能对应于缠绕或解缠绕的细丝。基于这一概念,提出了纺锤体微管行为和染色体后期运动的简单模型。假定后者是通过伴随动粒微管的螺旋细丝解缠绕而发生的,这会导致它们同时解聚。