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利用青蛙骨骼肌单纤维中的阶梯式缩短研究横桥动力学。

Cross-bridge kinetics studied with staircase shortening in single fibres from frog skeletal muscle.

作者信息

Linari M, Lombardi V, Piazzesi G

机构信息

Dipartimento di Scienze Fisiologiche, Università degli Studi di Firenze, Italy.

出版信息

J Muscle Res Cell Motil. 1997 Feb;18(1):91-101. doi: 10.1023/a:1018637118052.

Abstract

The kinetics of actin-myosin interaction has been studied in single active muscle fibres by repetitively eliciting tension transients with staircase shortening, consisting in a sequence of step releases of identical size (1-5 nm per half-sarcomere) imposed at regular time intervals (3-11 ms). Under sarcomere length-clamp conditions, the quick phase of tension recovery following each step in the staircase is the manifestation of the working stroke by synchronized cross-bridges. Different average shortening velocities are obtained by varying both the size of the step and the time interval between steps. Ti, the tension just before each step in the sequence, T2, the tension attained at the end of the quick phase of tension recovery, decrease with the number of steps, reaching a steady state value, which is lower the larger the shortening velocity. In agreement with previous results on tension response to steady shortening, the overall shortening necessary to approach the steady state values of Ti and T2 is about 15 nm. The normalized amplitude of quick tension recovery (T2r), which is measured by the ratio of the amount of tension recovered at the end of the quick phase (T2-T1) over the tension drop simultaneous with the step (Ti-T1), has been used to measure the extent of the working stroke elicited by each step in the staircase. The steady state value of T2r decreases progressively with the increase of shortening velocity. At velocities higher than 0.5 microns s-1 per half-sarcomere the steady state value of T2r is attained after a transitory depression, which reaches a maximum for an amount of overall shortening increasing from about 8 nm up to about 13 nm with increase in shortening velocity from 0.5 to 1.4 microns s-1 per half-sarcomere. The velocity-dependent transitory depression of T2r can be explained with the mechanical-kinetic model described previously. In the model cross-bridges cycle through two pathway distinct for the kinetics of the detachment/reattachment process. Shortening promotes a redistribution of cross-bridges interacting in the isometric conditions among the various states of the force-generating process. Shortening at high speed, preventing most of cross-bridges from undergoing the relatively fast (100 s-1) detachment/reattachment process, uncovers a rate limiting step in the cycle at the end of the 12 nm working stroke. Under these conditions, the finding that the fraction of the working stroke elicited by each step is transitory depressed with respect to the steady state value reveals that in the original isometric state a large fraction of interacting cross-bridges was accumulated near the beginning of the working stroke.

摘要

通过用阶梯式缩短重复引发张力瞬变,在单个活性肌纤维中研究了肌动蛋白 - 肌球蛋白相互作用的动力学。阶梯式缩短包括以规则的时间间隔(3 - 11毫秒)施加一系列相同大小(每个半肌节1 - 5纳米)的步长释放。在肌节长度钳制条件下,阶梯中每一步之后张力恢复的快速阶段是同步横桥工作行程的表现。通过改变步长大小和步长之间的时间间隔可获得不同的平均缩短速度。序列中每一步之前的张力Ti,以及在张力恢复快速阶段结束时达到的张力T2,随步数减少,达到一个稳态值,缩短速度越大该稳态值越低。与先前关于对稳定缩短的张力响应的结果一致,接近Ti和T2稳态值所需的总缩短量约为15纳米。快速张力恢复的归一化幅度(T2r)通过快速阶段结束时恢复的张力量(T2 - T1)与步长同时的张力下降(Ti - T1)的比值来测量,已被用于测量阶梯中每一步引发的工作行程的程度。T2r的稳态值随着缩短速度的增加而逐渐降低。在高于每个半肌节0.5微米/秒的速度下,T2r的稳态值在短暂下降后达到,随着缩短速度从每个半肌节0.5微米/秒增加到1.4微米/秒,整体缩短量从约8纳米增加到约13纳米时,短暂下降达到最大值。T2r的速度依赖性短暂下降可以用先前描述的机械 - 动力学模型来解释。在该模型中,横桥通过两个在分离/重新附着过程动力学上不同的途径循环。缩短促进了在等长条件下相互作用的横桥在力产生过程的各种状态之间的重新分布。高速缩短阻止了大多数横桥经历相对快速(100秒^-1)的分离/重新附着过程,在12纳米工作行程结束时揭示了循环中的一个限速步骤。在这些条件下,发现每一步引发的工作行程部分相对于稳态值短暂下降,这表明在原始等长状态下,很大一部分相互作用横桥聚集在工作行程开始附近。

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