Higuchi H, Goldman Y E
Department of Physiology, University of Pennsylvania, Philadelphia 19104-6083, USA.
Biophys J. 1995 Oct;69(4):1491-507. doi: 10.1016/S0006-3495(95)80020-2.
We measured isotonic sliding distance of single skinned fibers from rabbit psoas muscle when known and limited amounts of ATP were made available to the contractile apparatus. The fibers were immersed in paraffin oil at 20 degrees C, and laser pulse photolysis of caged ATP within the fiber initiated the contraction. The amount of ATP released was measured by photolyzing 3H-ATP within fibers, separating the reaction products by high-pressure liquid chromatography, and then counting the effluent peaks by liquid scintillation. The fiber stiffness was monitored to estimate the proportion of thick and thin filament sites interacting during filament sliding. The interaction distance, Di, defined as the sliding distance while a myosin head interacts with actin in the thin filament per ATP molecule hydrolyzed, was estimated from the shortening distance, the number of ATP molecules hydrolyzed by the myosin heads, and the stiffness. Di increased from 11 to 60 nm as the isotonic tension was reduced from 80% to 6% of the isometric tension. Velocity and Di increased with the concentration of ATP available. As isotonic load was increased, the interaction distance decreased linearly with decrease of the shortening velocity and extrapolated to 8 nm at zero velocity. Extrapolation of the relationship between Di and velocity to saturating ATP concentration suggests that Di reaches 100-190 nm at high shortening velocity. The interaction distance corresponds to the sliding distance while cross-bridges are producing positive (working) force plus the distance while they are dragging (producing negative forces). The results indicate that the working and drag distances increase as the velocity increases. Because Di is larger than the size of either the myosin head or the actin monomer, the results suggest that for each ATPase cycle, a myosin head interacts mechanically with several actin monomers either while working or while producing drag.
当已知且数量有限的三磷酸腺苷(ATP)作用于收缩装置时,我们测量了来自兔腰大肌的单根去表皮纤维的等张滑动距离。将纤维浸入20摄氏度的石蜡油中,通过对纤维内笼化ATP进行激光脉冲光解引发收缩。通过对纤维内的3H-ATP进行光解、用高压液相色谱法分离反应产物,然后通过液体闪烁计数流出峰来测量释放的ATP量。监测纤维的刚度以估计细丝滑动过程中相互作用的粗丝和细丝位点的比例。相互作用距离Di定义为每水解一个ATP分子时,肌球蛋白头部与细肌丝中的肌动蛋白相互作用时的滑动距离,通过缩短距离、肌球蛋白头部水解的ATP分子数量和刚度来估计。随着等张张力从等长张力的80%降至6%,Di从11纳米增加到60纳米。速度和Di随可用ATP浓度的增加而增加。随着等张负荷增加,相互作用距离随缩短速度的降低呈线性下降,在零速度时外推至8纳米。将Di与速度之间的关系外推到饱和ATP浓度表明,在高缩短速度下Di达到100 - 190纳米。相互作用距离对应于横桥产生正向(做功)力时的滑动距离加上它们拖动(产生负向力)时的距离。结果表明,做功和拖动距离随着速度的增加而增加。由于Di大于肌球蛋白头部或肌动蛋白单体的大小,结果表明在每个ATP酶循环中,一个肌球蛋白头部在做功或产生拖动时与几个肌动蛋白单体发生机械相互作用。