Dupuis D E, Guilford W H, Wu J, Warshaw D M
Department of Molecular Physiology and Biophysics, University of Vermont, Burlington 05405, USA.
J Muscle Res Cell Motil. 1997 Feb;18(1):17-30. doi: 10.1023/a:1018672631256.
Numerous biological processes, including muscular contraction, depend upon the mechanical properties of actin filaments. One such property is resistance to bending (flexural rigidity, EI). To estimate EI, we attached the ends of fluorescently labelled actin filaments to two microsphere 'handles' captured in independent laser traps. The positions of the traps were manipulated to apply a range of tensions (0-8 pN) to the filaments via the microsphere handles. With increasing filament tension, the displacement of the microspheres was inconsistent with a microsphere-filament system that is rigid. We maintain that this inconsistency is due to the microspheres rotating in the trap and the filaments bending near either attachments to accommodate this rotation. Fitting the experimental data to a simple model of this phenomena, we estimate actin's EI to be approximately 15 x 10(3) pNnm2, a value within the range of previously reported results, albeit using a novel method. These results both: support the idea that actin filaments are more compliant than historically assumed; and, indicate that without appropriately pretensioning the actin filament in similar laser traps, measurements of unitary molecular events (e.g. myosin displacement) may be significantly underestimated.
许多生物过程,包括肌肉收缩,都依赖于肌动蛋白丝的力学特性。其中一个特性是抗弯曲性(弯曲刚度,EI)。为了估计EI,我们将荧光标记的肌动蛋白丝的末端连接到捕获在独立激光阱中的两个微球“手柄”上。通过微球手柄操纵阱的位置,对丝施加一系列张力(0 - 8 pN)。随着丝张力的增加,微球的位移与刚性的微球 - 丝系统不一致。我们认为这种不一致是由于微球在阱中旋转以及丝在靠近任何一个附着点处弯曲以适应这种旋转。将实验数据拟合到这种现象的一个简单模型中,我们估计肌动蛋白的EI约为15×10³ pNnm²,尽管使用了一种新方法,但该值在先前报道的结果范围内。这些结果都:支持肌动蛋白丝比以往认为的更具柔韧性的观点;并且表明,如果在类似的激光阱中不对肌动蛋白丝进行适当的预张紧,单一分子事件(如肌球蛋白位移)的测量可能会被显著低估。