Force-velocity relationship of single actin filament interacting with immobilised myosin measured by electromagnetic technique.

S-J P Holohan, S B Marston
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引用次数: 8

Abstract

The effect of applying an external load to actin filaments moving in the in vitro motility assay is studied. Bead-tailed actin filaments were made by polymerising actin onto 2.8 microm diameter Dynabeads conjugated with gelsolin-G actin. These were introduced into a motility cell coated with 100 microg/ml rabbit fast skeletal myosin in the presence of ATP and 0.5% methylcellulose. The motility cell was inserted between the pole-pieces of an electromagnet and the fluorescent beads and filaments were observed. The force-current relationship of the electromagnet was determined from the velocity of free beads in viscous solution and Stokes' equation. The magnet produced up to 6 pN force on the Dynabeads at 1 A. Many bead-tailed actin filaments stuck to the surface, but the beads that did move moved at the same speed as unloaded f-actin in the same cell. Bead-tailed filaments slowed down under an increasing magnetic load, eventually stalled and then slid backward under increasing load before detaching from the surface. Single-filament force-velocity curves were constructed and a stalling force of about 0.6 pN/mm of actin filament estimated.

电磁法测定肌动蛋白单丝与固定肌球蛋白相互作用的力-速度关系。
在体外运动试验中,研究了施加外部负荷对肌动蛋白丝运动的影响。将肌动蛋白聚合到直径为2.8微米的与胶凝蛋白- g肌动蛋白偶联的dynabheads上,制成了束尾肌动蛋白丝。在ATP和0.5%甲基纤维素的存在下,将这些细胞引入涂有100微克/毫升兔快速骨骼肌球蛋白的运动细胞中。将运动细胞插入电磁铁的极片之间,观察荧光珠和荧光丝。根据黏性溶液中自由磁珠的速度和Stokes方程确定了电磁铁的力流关系。磁铁在1a时对dynabead产生高达6pn的力。许多束状的肌动蛋白丝粘附在细胞表面,但在同一细胞中,这些束状的肌动蛋白丝的移动速度与未装载的f-肌动蛋白相同。在不断增加的磁载荷作用下,珠尾细丝变慢,最终停滞,然后在不断增加的载荷作用下向后滑动,最后脱离表面。构建了单丝力-速度曲线,估计肌动蛋白丝的失速力约为0.6 pN/mm。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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