Borejdo J, Shepard A, Akopova I, Grudzinski W, Malicka J
Department of Molecular Biology and Immunology, University of North Texas, Fort Worth, Texas 76107, USA.
Biophys J. 2004 Dec;87(6):3912-21. doi: 10.1529/biophysj.104.045450. Epub 2004 Sep 17.
The rotation of the lever arm of myosin cross-bridges is believed to be responsible for muscle contraction. To resolve details of this rotation, it is necessary to observe a single cross-bridge. It is still impossible to do so in muscle fiber, but it is possible to investigate a small population of cross-bridges by simultaneously activating myosin in a femtoliter volume by rapid release of caged ATP. In earlier work, in which the number of observed cross-bridges was limited to approximately 600 by confocal microscopy, we were able to measure the rates of cross-bridge detachment and rebinding. However, we were unable to resolve the power stroke. We speculated that the reason for this was that the number of observed cross-bridges was too large. In an attempt to decrease this number, we used two-photon microscopy which permitted observation of approximately 1/2 as many cross-bridges as before with the same signal/noise ratio. With the two-photon excitation, the number of cross-bridges was small enough to resolve the beginning of the power stroke. The results indicated that the power stroke begins approximately 170 ms after the rigor cross-bridge first binds ATP.
肌球蛋白横桥的杠杆臂旋转被认为是肌肉收缩的原因。为了解析这种旋转的细节,有必要观察单个横桥。在肌肉纤维中仍然无法做到这一点,但通过快速释放笼锁ATP在飞升体积内同时激活肌球蛋白,可以研究一小群横桥。在早期的工作中,通过共聚焦显微镜观察到的横桥数量限制在大约600个,我们能够测量横桥解离和重新结合的速率。然而,我们无法解析动力冲程。我们推测原因是观察到的横桥数量太多。为了减少这个数量,我们使用了双光子显微镜,在相同信噪比的情况下,它允许观察到的横桥数量大约是以前的1/2。通过双光子激发,横桥数量足够少,能够解析动力冲程的开始。结果表明,动力冲程在强直横桥首次结合ATP后约170毫秒开始。