Tözeren A, Schoenberg M
Biophys J. 1986 Nov;50(5):875-84. doi: 10.1016/S0006-3495(86)83528-7.
The effect of cross-bridge clustering and head-head competition on the mechanical response of skeletal muscle under equilibrium conditions is considered. For this purpose, the recent multiple site equilibrium cross-bridge model of Schoenberg (Schoenberg, M., 1985, Biophys. J., 48:467-475) is extended in accordance with the formalism of T.L. Hill (1974, Prog. Biophys, Mol. Biol., 28:267-340) to consider the case where groups of independent cross-bridge heads compete with each other for binding to multiple actin sites. Cooperative behavior between heads is not allowed. Computations indicate that for the double-headed cross-bridge with two independent equivalent heads, the time course of force decay after a stretch is similar to that for the single-headed cross-bridge; that is, the rate constant for force decay is approximately equal to the cross-bridge head detachment rate constant. The results also show that the force decay after a stretch becomes slower than the detachment rate constant of a single head when cross-bridge heads bind adjacently in clusters so that competition between heads for binding to the available actin sites increases. However, if one assumes that the detachment rate constant of an unstrained head in a fiber is comparable to that of an S1 molecule in solution, this effect is not large enough to explain why some of the rate constants for force decay after a stretch in rigor, or in the presence of ATP analogues such as adenyl-5'-yl imidodiphosphate, appear to be significantly slower than the detachment rate constant of S1 from actin in solution.
研究了平衡条件下横桥聚类和头对头竞争对骨骼肌力学响应的影响。为此,根据T.L.希尔(1974年,《生物物理学进展,分子生物学》,28:267 - 340)的形式体系,扩展了Schoenberg最近的多位点平衡横桥模型(Schoenberg,M.,1985年,《生物物理学杂志》,48:467 - 475),以考虑多组独立横桥头部相互竞争结合多个肌动蛋白位点的情况。不允许头部之间存在协同行为。计算表明,对于具有两个独立等效头部的双头横桥,拉伸后力衰减的时间进程与单头横桥相似;即,力衰减的速率常数大约等于横桥头部脱离速率常数。结果还表明,当横桥头部以簇状相邻结合,使得头部之间对结合可用肌动蛋白位点的竞争增加时,拉伸后的力衰减变得比单个头部的脱离速率常数更慢。然而,如果假设纤维中未受应变的头部的脱离速率常数与溶液中S1分子的脱离速率常数相当,那么这种效应不足以解释为什么在僵直状态下或存在ATP类似物(如腺苷 - 5'-亚氨二磷酸)时,一些拉伸后力衰减的速率常数似乎明显慢于溶液中S1从肌动蛋白上的脱离速率常数。