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完整公牛精子鞭毛在等长阻滞时产生的力的测量以及动力蛋白失速力的估计。

Measurement of the force produced by an intact bull sperm flagellum in isometric arrest and estimation of the dynein stall force.

作者信息

Schmitz K A, Holcomb-Wygle D L, Oberski D J, Lindemann C B

机构信息

Department of Biological Sciences, Oakland University, Rochester, Michigan 48309-4476, USA.

出版信息

Biophys J. 2000 Jul;79(1):468-78. doi: 10.1016/S0006-3495(00)76308-9.

Abstract

The force generated by a detergent-extracted reactivated bull sperm flagellum during an isometric stall was measured with a force-calibrated glass microprobe. The average isometric stall force from 48 individual measurements was 2.5 +/- 0.7 x 10(-5) dyne (2.5 +/- 0.7 x 10(-10) N). The force measurements were obtained by positioning a calibrated microprobe in the beat path of sperm cells that were stuck by their heads to a glass microscope slide. The average position of the contact point of the flagellum with the probe was 15 microm from the head-tail junction. This average lever arm length multiplied by the measured force yields an estimate of the active bending moment (torque) of 3.9 x 10(-8) dyne x cm (3.9 x 10(-15) N x m). The force was sustained and was for the most part uniform, despite the fact that the flagellum beyond the point of contact with the probe usually continued beating. It appears that the dynein motors in the basal portion of the flagellum continue to pull in an isometric stall for as long as the motion of the flagellum is blocked. If dynein motors in the flagellum distal to the contact point with the probe were contributing force to the displacement of the probe, then the flagellar segment immediately past the point of contact would have to show a net curvature in the direction of the probe displacement. No such curvature bias was observed in the R-bend arrests, and only a small positive curvature bias was measured in the P-bend arrests. Our analysis of the data suggests that more than 90% of the sustained force component is generated by the part of the flagellum between the probe and the flagellar base. Based on this premise, the isometric stall force per dynein head is estimated to be 5.0 x 10(-7) dyne (5 pN). This equals approximately 1.0 x 10(-6) dyne (10 pN) per intact dynein arm. These values are close to the isometric stall force of isolated dynein. This suggests that all of the dynein heads between the base and the probe, on the active side of the axoneme, are contributing to the force exerted against the probe.

摘要

用经过力校准的玻璃微探针测量了去污剂提取后再激活的公牛精子鞭毛在等长停滞期间产生的力。48次单独测量得到的平均等长停滞力为2.5±0.7×10⁻⁵达因(2.5±0.7×10⁻¹⁰牛)。通过将校准后的微探针置于头部粘在玻璃显微镜载玻片上的精子细胞的摆动路径中来获得力的测量值。鞭毛与探针接触点的平均位置距离头尾连接处15微米。这个平均力臂长度乘以测量到的力得出的主动弯曲力矩(扭矩)估计值为3.9×10⁻⁸达因·厘米(3.9×10⁻¹⁵牛·米)。尽管与探针接触点之外的鞭毛通常继续摆动,但力是持续的且在很大程度上是均匀的。似乎只要鞭毛的运动被阻断,鞭毛基部的动力蛋白马达就会在等长停滞状态下持续拉动。如果与探针接触点远端的鞭毛中的动力蛋白马达对探针的位移有作用力,那么紧挨着接触点的鞭毛段就会在探针位移方向上显示出净曲率。在R型弯曲停滞中未观察到这种曲率偏差,在P型弯曲停滞中仅测量到小的正曲率偏差。我们对数据的分析表明,超过90%的持续力分量是由探针和鞭毛基部之间的鞭毛部分产生的。基于这个前提,每个动力蛋白头部的等长停滞力估计为5.0×10⁻⁷达因(5皮牛)。这相当于每个完整的动力蛋白臂约1.0×10⁻⁶达因(10皮牛)。这些值接近分离的动力蛋白的等长停滞力。这表明轴丝活动侧基部和探针之间的所有动力蛋白头部都在对施加在探针上的力有贡献。

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